courtlistener_docket
41 records
Williams v. Angiodynamics, Inc.
2026-06-02
Federal docket 3:26-cv-03351 (casd); matched party 'Angiodynamics, Inc.'
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Daniels v. AngioDynamics, Inc.
2026-06-01
Federal docket 3:26-cv-03337 (casd); matched party 'AngioDynamics, Inc.'
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Walters v. AngioDynamics, Inc.
2026-05-28
Federal docket 3:26-cv-03285 (casd); matched party 'AngioDynamics, Inc.'
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Hedges v. Angiodynamics, Inc.
2026-05-28
Federal docket 3:26-cv-03271 (casd); matched party 'Angiodynamics, Inc.'
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Brown v. AngioDynamics, Inc.
2026-05-27
Federal docket 3:26-cv-03263 (casd); matched party 'AngioDynamics, Inc.'
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Good v. Angiodynamics, Inc.
2026-05-21
Federal docket 3:26-cv-03185 (casd); matched party 'Angiodynamics, Inc.'
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Perkins v. Angiodynamics, Inc.
2026-05-21
Federal docket 3:26-cv-03184 (casd); matched party 'Angiodynamics, Inc.'
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Whiteford v. Angiodynamics, Inc.
2026-05-21
Federal docket 3:26-cv-03175 (casd); matched party 'Angiodynamics, Inc.'
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Marshall v. Angiodynamics, Inc.
2026-05-15
Federal docket 3:26-cv-03054 (casd); matched party 'Angiodynamics, Inc.'
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Borrego v. Angiodynamics, Inc.
2026-05-14
Federal docket 3:26-cv-03035 (casd); matched party 'Angiodynamics, Inc.'
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Williams v. Angiodynamics, Inc.
2026-05-14
Federal docket 3:26-cv-03030 (casd); matched party 'Angiodynamics, Inc.'
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Chesser v. Angiodynamics, Inc.
2026-05-13
Federal docket 3:26-cv-03004 (casd); matched party 'Angiodynamics, Inc.'
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Lochmann v. Angiodynamics, Inc.
2026-05-11
Federal docket 3:26-cv-02953 (casd); matched party 'Angiodynamics, Inc.'
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Roberts v. Angiodynamics, Inc.
2026-05-07
Federal docket 3:26-cv-02886 (casd); matched party 'Angiodynamics, Inc.'
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Ray v. Angiodynamics, Inc.
2026-05-05
Federal docket 3:26-cv-02840 (casd); matched party 'Angiodynamics, Inc.'
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Lawrence v. Angiodynamics, Inc.
2026-05-05
Federal docket 3:26-cv-02839 (casd); matched party 'Angiodynamics, Inc.'
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Eichler v. Angiodynamics, Inc.
2026-05-04
Federal docket 3:26-cv-02810 (casd); matched party 'Angiodynamics, Inc.'
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Lopez v. Angiodynamics, Inc.
2026-05-01
Federal docket 3:26-cv-02780 (casd); matched party 'Angiodynamics, Inc.'
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Carte v. Angiodynamics, Inc.
2026-04-30
Federal docket 3:26-cv-02740 (casd); matched party 'Angiodynamics, Inc.'
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Siler v. Angiodynamics, Inc.
2026-04-29
Federal docket 3:26-cv-02709 (casd); matched party 'Angiodynamics, Inc.'
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Fancher v. Angiodynamics, Inc.
2026-04-27
Federal docket 3:26-cv-02661 (casd); matched party 'Angiodynamics, Inc.'
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Ortega v. Angiodynamics, Inc.
2026-04-24
Federal docket 3:26-cv-02603 (casd); matched party 'Angiodynamics, Inc.'
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AngioDynamics, Inc. v. Endovascular Engineering, Inc.
2026-04-23
Federal docket 1:26-cv-00469 (ded); matched party 'AngioDynamics, Inc.'
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Adams v. Angiodynamics, Inc.
2026-04-21
Federal docket 3:26-cv-02536 (casd); matched party 'Angiodynamics, Inc.'
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Bunch v. AngioDynamics, Inc.
2026-04-21
Federal docket 3:26-cv-02528 (casd); matched party 'AngioDynamics, Inc.'
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Cannon v. Angiodynamics, Inc.
2026-04-21
Federal docket 3:26-cv-02511 (casd); matched party 'Angiodynamics, Inc.'
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Test v. Angiodynamics, Inc.
2026-04-20
Federal docket 3:26-cv-02501 (casd); matched party 'Angiodynamics, Inc.'
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Henderson v. Angiodynamics, Inc.
2026-04-20
Federal docket 3:26-cv-02484 (casd); matched party 'Angiodynamics, Inc.'
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Noon v. Angiodynamics, Inc.
2026-04-15
Federal docket 3:26-cv-02391 (casd); matched party 'Angiodynamics, Inc.'
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Bradshaw v. Angiodynamics, Inc.
2026-04-10
Federal docket 3:26-cv-02271 (casd); matched party 'Angiodynamics, Inc.'
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Harden v. Angiodynamics, Inc.
2026-04-09
Federal docket 3:26-cv-02253 (casd); matched party 'Angiodynamics, Inc.'
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Larson v. Angiodynamics, Inc.
2026-04-09
Federal docket 3:26-cv-02252 (casd); matched party 'Angiodynamics, Inc.'
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Rhone v. Angiodynamics, Inc.
2026-04-02
Federal docket 3:26-cv-02074 (casd); matched party 'Angiodynamics, Inc.'
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Brown v. Angiodynamics, Inc.
2026-04-01
Federal docket 3:26-cv-02064 (casd); matched party 'Angiodynamics, Inc.'
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Stachura v. Angiodynamics, Inc.
2026-04-01
Federal docket 3:26-cv-02058 (casd); matched party 'Angiodynamics, Inc.'
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Peace v. Angiodynamics, Inc.
2026-04-01
Federal docket 3:26-cv-02060 (casd); matched party 'Angiodynamics, Inc.'
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Dimond v. Angiodynamics, Inc.
2026-03-30
Federal docket 3:26-cv-01998 (casd); matched party 'Angiodynamics, Inc.'
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Krawl v. Angiodynamics, Inc.
2026-03-30
Federal docket 3:26-cv-01996 (casd); matched party 'Angiodynamics, Inc.'
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Thompson v. Angiodynamics, Inc.
2026-03-27
Federal docket 3:26-cv-01960 (casd); matched party 'Angiodynamics, Inc.'
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Armstrong v. Angiodynamics, Inc.
2026-03-26
Federal docket 3:26-cv-01912 (casd); matched party 'Angiodynamics, Inc.'
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Majors v. Angiodynamics, Inc.
2026-03-25
Federal docket 3:26-cv-01897 (casd); matched party 'Angiodynamics, Inc.'
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fda
73 records
FDA Recall: Angiodynamics, Inc. — Class II
20260429
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) o | Product: Soft-Vu Angiographic Catheter, Kumpe, ...
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FDA Recall: Angiodynamics, Inc. — Class II
20260429
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) o | Product: AccuVu Angiographic Catheter, Straight...
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FDA Recall: Angiodynamics, Inc. — Class II
20260429
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) o | Product: Soft-Vu Angiographic Catheter, Berenst...
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FDA Device Recall: AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-
2025-01-08
Class II — Potential for procedural delays or interruptions during use of the Auryon Atherectomy System due to the Auryon Atherectomy System not advancing to the Activation (Ready) mode.
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FDA Recall: Angiodynamics, Inc. — Class II
20240807
Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a di | Product: SOFT-VU KUMPE 5F X 40CM -Used for pati...
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FDA Recall: Angiodynamics, Inc. — Class II
20240515
Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical pro | Product: DURAFLOW 2, 32CM STRAIGHT BASIC KIT ...
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FDA Recall: Angiodynamics, Inc. — Class II
20240515
Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical pro | Product: DURAMAX STACKED TIP 32CM STR. BASIC KI...
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FDA Recall: Angiodynamics, Inc. — Class II
20240327
Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass | Product: MINI STICK MAX 5F X 10 CM STD .018 NI/...
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FDA Recall: Angiodynamics, Inc. — Class II
20240327
Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass | Product: MINI STICK MAX 5F X 10 CM STD .018 SS/...
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FDA Recall: Angiodynamics, Inc. — Class II
20240327
Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass | Product: MINI STICK MAX 4F X 10 CM STD .018 NI/...
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FDA Recall: Angiodynamics, Inc. — Class II
20240214
Rotating adaptor O-ring manufacturing defect impacting seal integrity which may lead to a leak during infusion of medication. | Product: PulseSpray Infusion System devices including: PULSE SPRAY 5F/13...
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FDA Device Recall: SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. C
2024-08-07
Class II — Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a different model (catheter length)
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FDA Device Recall: IsoLoc Prostate Immobilization Treatment Balloon Device Kit, Catalog/UPN: ISO-10
2024-07-10
Class II — A single batch of ISO-100 IsoLoc Gas-Release Endorectal Balloons is mislabeled. The affected ISO-100 balloon catheter has a nominal fill volume of 100cc/ml but the inner pouch identifies t...
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FDA Device Recall: DURAFLOW 2, 32CM STRAIGHT BASIC KIT PG-Indicated for use in attaining Long-Ter
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
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FDA Device Recall: DURAMAX STACKED TIP 32CM STR. BASIC KIT, 5-UP PG- Indicated for use in attaining
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
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FDA Device Recall: DURAMAX STACKED TIP 24CM STR. BASIC KIT, 1-UP PG Product Number: H78710302803
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
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FDA Device Recall: DURAMAX STACKED TIP 28CM STR. BASIC KIT, 1-UP PG- Indicated for use in attaining
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
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FDA Device Recall: DURAFLOW 2, 24CM STRAIGHT BASIC KIT -Indicated for use in attaining Long-Term va
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
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FDA Device Recall: DURAFLOW 2, 55CM STRAIGHT BASIC KIT PG- Indicated for use in attaining Long-Te
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
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FDA Device Recall: BioFlo DuraMax 15.5F 24cm Single Valve Sheath VascPak Kit- Indicated for use in
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
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FDA Device Recall: DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK, 1-UP PG- Indicated for use in att
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
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FDA Device Recall: DURAMAX STACKED TIP 32 CM STRAIGHT VASC-PAK, 1-UP PG- Indicated for use in atta
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
View Source
FDA Device Recall: DURAFLOW 2, 28CM STRAIGHT VASC-PAK PG- Indicated for use in attaining Long-Ter
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
View Source
FDA Device Recall: DURAMAX STACKED TIP 28CM STR. BASIC KIT, 5-UP PG- Indicated for use in attaining
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
View Source
FDA Device Recall: DURAFLOW 2, 24CM STRAIGHT VASC-PAK PG- Indicated for use in attaining Long-Ter
2024-05-15
Class II — Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
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FDA Device Recall: MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneou
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
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FDA Device Recall: MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 1.6" PG- Used for the percutaneous
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
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FDA Device Recall: MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
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FDA Device Recall: MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
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FDA Device Recall: MINI STICK MAX 4F X 10 CM STD .018 SS/PD ECHO 2.75" PG-Used for the percutaneous
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
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FDA Device Recall: MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneo
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
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FDA Device Recall: MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneo
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
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FDA Device Recall: MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG- Used for the percut
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
View Source
FDA Device Recall: MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneo
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
View Source
FDA Device Recall: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- Used for the percutaneou
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
View Source
FDA Device Recall: MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutan
2024-03-27
Class II — Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the pr...
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FDA Device Recall: PulseSpray Infusion System devices including: PULSE SPRAY 5F/135/20, UPN: H78712
2024-02-14
Class II — Rotating adaptor O-ring manufacturing defect impacting seal integrity which may lead to a leak during infusion of medication.
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FDA Device Recall: Vortex MP Port Titanium Low Profile Implanted Port with 5F attached Silicone Cat
2022-11-02
Class II — Printed Instructions for Use (IFU) not shipped with device. The Instructions for Use contain the Warnings, Precautions, Contraindications, and Procedures for the Preparation, Implantation, ...
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FDA Recall: Angiodynamics, Inc. — Class II
20210915
Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can oc | Product: Solero Generator US PG, Item No. H7871...
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FDA Device Recall: Solero Generator US PG, Item No. H78712740000US0, Catalog No. 12740000US
2021-09-15
Class II — Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up.
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FDA Device Recall: Solero Generator Refurbished US PG, Item No. H78712740000USD0, Catalog No. 12740
2021-09-15
Class II — Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up.
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FDA Recall: Angiodynamics, Inc. — Class II
20200624
Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020. | Product: BioFlo Midline Convenience Kits - Product Usage: These int...
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FDA Device Recall: BioFlo Midline Convenience Kits - Product Usage: These introducers are used for
2020-06-24
Class II — Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020.
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FDA Device Recall: BioFlo PICC and Xcela PICC Maximal Barrier Nursing Kits - Product Usage: are ind
2020-06-24
Class II — Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020.
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FDA Device Recall: BioFlo PICC and Xcela PICC Convenience Kits - Product Usage: are indicated for s
2020-06-24
Class II — Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020.
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FDA Device Recall: BioFlo Midline Catheter and BioFlo Maximal Barrier Kits - Product Usage: These i
2020-06-24
Class II — Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020.
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FDA Device Recall: OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT, Catalog Number:
2019-12-25
Class II — May result in readings outside of the expected accuracy range.
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FDA Device Recall: OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product Usage
2019-12-25
Class II — May result in readings outside of the expected accuracy range.
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FDA Device Recall: MICRO-PSD HDR, Catalog Number: PSD-HB5N - Product Usage: pre-calibrated PSD sens
2019-12-25
Class II — May result in readings outside of the expected accuracy range.
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FDA Device Recall: Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015); SV OF 5F x 65 cm .
2018-03-07
Class II — Product was placed into distribution prior to completion of all required post sterilization release activities.
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FDA Device Recall: Accu2i pMTA Applicator, 19 cm INTERMEDIATE, REF/Catalog # 900-602-US, Model # (
2018-02-14
Class II — The firm is recalling product that has the potential to not function during use. The product affected by this recall will not deliver the desired microwave energy due to coolant ingress i...
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FDA Device Recall: Accu2i pMTA Applicator, 19 cm INTERMEDIATE, REF/Catalog # 900-602, Model # (UPN
2018-02-14
Class II — The firm is recalling product that has the potential to not function during use. The product affected by this recall will not deliver the desired microwave energy due to coolant ingress i...
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FDA Device Recall: Accu2i pMTA Applicator, 14 cm STANDARD, REF/Catalog # 900-600-US, Model # (UPN)
2018-02-14
Class II — The firm is recalling product that has the potential to not function during use. The product affected by this recall will not deliver the desired microwave energy due to coolant ingress i...
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FDA Device Recall: Accu2i pMTA Applicator, 29 cm LONG, REF/Catalog # 900-601-US, Model # (UPN) H78
2018-02-14
Class II — The firm is recalling product that has the potential to not function during use. The product affected by this recall will not deliver the desired microwave energy due to coolant ingress i...
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FDA Device Recall: Accu2i pMTA Applicator, 29 cm LONG, REF/Catalog # 900-601, Model # (UPN) H78790
2018-02-14
Class II — The firm is recalling product that has the potential to not function during use. The product affected by this recall will not deliver the desired microwave energy due to coolant ingress i...
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FDA Recall: Angiodynamics, Inc. — Class III
20161228
Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator components has determined that the products listed in their September 7, 2016 Reca | Product: ANGIODYNAMICS Percutaneous Introducer ...
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FDA Device Recall: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Sti
2016-12-28
Class III — Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator components has determined that the products listed in their September 7, 2016 Recall Notification have the potential for...
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FDA Device Recall: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Sti
2016-12-28
Class III — Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator components has determined that the products listed in their September 7, 2016 Recall Notification have the potential for...
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FDA Device Recall: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Sti
2016-12-28
Class III — Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator components has determined that the products listed in their September 7, 2016 Recall Notification have the potential for...
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FDA Device Recall: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Sti
2016-12-28
Class II — Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator components has determined that the products listed in their September 7, 2016 Recall Notification have the potential for ...
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FDA Device Recall: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Sti
2016-12-28
Class III — Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator components has determined that the products listed in their September 7, 2016 Recall Notification have the potential for...
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FDA Device Recall: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Sti
2016-12-28
Class III — Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator components has determined that the products listed in their September 7, 2016 Recall Notification have the potential for...
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FDA Device Recall: NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK, REF Catalog No. 6519
2016-04-13
Class II — Procedure Products initiated the recall due to the inner lumen of the needles not meeting the intended specification. Specifically, at least a portion of the affected lot is unable to acce...
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FDA Device Recall: NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT, REF Catalog No. 601319
2016-04-13
Class II — Procedure Products initiated the recall due to the inner lumen of the needles not meeting the intended specification. Specifically, at least a portion of the affected lot is unable to acce...
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FDA Device Recall: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT, REF Catalog No. 60
2016-04-13
Class II — Procedure Products initiated the recall due to the inner lumen of the needles not meeting the intended specification. Specifically, at least a portion of the affected lot is unable to acce...
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FDA Device Recall: Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product
2015-03-04
Class II — Printed mark on the trocar intended to indicate a 5cm distance from the distal tip of the needle is actually located 4cm from the distal tip of the needle.
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FDA Recall: Angiodynamics, Inc. — Class II
20140827
AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long). | Product: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, ...
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FDA Device Recall: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 10 cm Infusion Pattern,
2014-08-27
Class II — AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long).
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FDA Device Recall: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 40 cm Infusion Pattern,
2014-08-27
Class II — AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long).
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FDA Device Recall: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 30 cm Infusion Pattern,
2014-08-27
Class II — AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long).
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FDA Recall: Angiodynamics, Inc. — Class II
20130605
AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT NeverTouch Procedure Kits, because the potential exists that the micro Introd | Product: AngioDynamics Micro Introducer Kits un...
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FDA Device Recall: AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables
2013-07-17
Class II — The RITA Main Cable product contains the incorrect Instructions for Use.
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FDA Device Recall: AngioDynamics Micro Introducer Kits under the following labeling: 1) AngioDyna
2013-06-05
Class II — AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT NeverTouch Procedure Kits, because the potential exists that the micro Introducer (sheath/dilator) packaged within t...
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ny_corps
1 records
NY Corp: ANGIODYNAMICS, INC.
1997-01-17
FOREIGN BUSINESS CORPORATION | County: Warren | Jurisdiction: Delaware
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SEC EDGAR
1 records
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