Department of Justice
1 records
DOJ: CareFusion to Pay the Government $40.1 Million
to Resolve Allegations That Include More Than $11 Million in Kickbacks to One Doctor 2014-01-09
to Resolve Allegations That Include More Than $11 Million in Kickbacks to One Doctor 2014-01-09
CareFusion Corp. has agreed to pay the government $40.1 million to settle allegations that it violated the False Claims Act by paying kickbacks and promoting its products for uses that were not approv...
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fda
22 records
FDA Recall: CAREFUSION — Class II
20220928
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is | Product: BD MaxGuard Drop Administration set wi...
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FDA Recall: CAREFUSION — Class II
20220928
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is | Product: BD MaxGuard 15 Drop Administration Set...
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FDA Device Recall: BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port M
2022-09-28
Class II — Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may ...
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FDA Device Recall: BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433
2022-09-28
Class II — Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may ...
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FDA Device Recall: BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9
2022-09-28
Class II — Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may ...
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FDA Device Recall: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS141
2022-09-28
Class II — Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may ...
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FDA Device Recall: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS106
2022-09-28
Class II — Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may ...
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FDA Recall: CAREFUSION — Class II
20210922
Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial | Product: BD Gravity Burette Set 60 DROP 1.2 MF ...
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FDA Recall: CAREFUSION — Class II
20210922
Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial | Product: BD Gravity IV Set 3-port Closed Manifo...
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FDA Device Recall: BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Device Recall: BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free Y-sites,
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Device Recall: BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Device Recall: BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Tubing SmartSit
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Device Recall: BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Device Recall: BD SmartSite Bag Access Device, REF: 2300E-0500; BD BAG ACCESS DEVICE CHECK VALV
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Device Recall: BD SmartSite 'Y' Extension Set 2 Needle-Free Valves, REF: 20019E7D
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Device Recall: BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED, REF: 42163E
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Device Recall: BD SmartSite, REF: 2000E CHINA; BD SmartSite Connector, REF: 2000E-04; BD SmartS
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Device Recall: BD Syringe Set 20 DP MIC TBG 0.2MF CKV Anti-Siphon SmartSite VLV Sensing Disc, R
2021-09-22
Class II — Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead ...
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FDA Recall: CareFusion Corporation — Class II
20130403
The recall was initiated because Carefusion has confirmed that when the PAS 2000 drawers due to inaccessability of drawers caused by system down time | Product: Pyxis Anesthesia System Model 2000 (PA...
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FDA Device Recall: Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alar
2013-04-24
Class I — The recall was initiated because Carefusion has received reports of a communication error on the Alaris PC unit model 8015 with software version 9.12 when the Alaris EtCO2 module or Alaris S...
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FDA Device Recall: Pyxis Anesthesia System Model 2000 (PAS 2000) Product Usage: The PAS 2000
2013-04-03
Class II — The recall was initiated because Carefusion has confirmed that when the PAS 2000 drawers due to inaccessability of drawers caused by system down time or lock-up.
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