EPA (Environmental Protection Agency)
1 records
epa_echo
2 records
fda
10 records
FDA Device Recall: Dialysate Concentrate for Hemodialysis-Liquid/Powd - Product Usage: used in conj
2021-06-23
Class II — The lot may have experienced an anomaly during the manufacturing process, that could lead to an out of specification concentrate formulation.
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FDA Recall: Medivators, Inc. — Class II
20200429
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of | Product: Medivators Endo Smartcap Endoscope Tub...
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FDA Recall: Medivators, Inc. — Class II
20200429
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of | Product: Medivators Endo carry-on Procedure Ki...
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FDA Recall: Medivators, Inc. — Class II
20200429
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of | Product: Medivators EndoGator REF 100651. Kit ...
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FDA Device Recall: Medivators Endo Smartcap Endoscope Tubing. REF100145CO2EXTU, packaged as Conte
2020-04-29
Class II — Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap t...
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FDA Device Recall: Medivators Endo carry-on Procedure Kit REF CPK-100222-0002 - Product Usage: is
2020-04-29
Class II — Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap t...
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FDA Device Recall: Medivators EndoGator REF 100651. Kit for Olympus 140/160/180/190 Series GI Endo
2020-04-29
Class II — Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap t...
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FDA Device Recall: Medivators EndoGator REF 100650. Kit for Olympus 140/160/180/190 Series GI Endo
2020-04-29
Class II — Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap t...
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FDA Device Recall: Medivators Endo Smartcap Endoscope Tubing. REF100145CO2, packaged as Contents
2020-04-29
Class II — Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap t...
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FDA Device Recall: Medivators Endo Smartcap Endoscope Tubing. REF100145CO2EXT, packaged as Conten
2020-04-29
Class II — Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap t...
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ny_corps
1 records
NY Corp: MEDIVATORS INC.
2001-11-26
FOREIGN BUSINESS CORPORATION | County: New York | Jurisdiction: Minnesota
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