Class IIOngoingZ-1057-2025
Karl Storz Endoscopy recalls KARL STORZ - ENDOSKOPE
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Karl Storz EndoscopyCAFeb 5, 2025
Recalls in California
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 361–372 of 439 recalls
Class IIOngoingZ-1056-2025
Karl Storz Endoscopy recalls KARL STORZ - ENDOSKOPE
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Karl Storz EndoscopyCAFeb 5, 2025
Class IIOngoingZ-1055-2025
Karl Storz Endoscopy recalls KARL STORZ - ENDOSKOPE
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Karl Storz EndoscopyCAFeb 5, 2025
Class IIOngoingZ-1054-2025
Karl Storz Endoscopy recalls KARL STORZ - ENDOSKOPE
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Karl Storz EndoscopyCAFeb 5, 2025
Class IIOngoingZ-1053-2025
Karl Storz Endoscopy recalls KARL STORZ - ENDOSKOPE
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Karl Storz EndoscopyCAFeb 5, 2025
Class IIOngoingZ-1052-2025
Karl Storz Endoscopy recalls KARL STORZ - ENDOSKOPE
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Karl Storz EndoscopyCAFeb 5, 2025
Class IIOngoingZ-1051-2025
Karl Storz Endoscopy recalls KARL STORZ - ENDOSKOPE
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Karl Storz EndoscopyCAFeb 5, 2025
Class IIOngoingZ-1050-2025
CareFusion 303, Inc. recalls BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 31…
Due to an increase in complaints of door latch assembly failures that may cause the doors to be left in an open state potentially causing inventory discrepancies, a delay in access to medication and/or diversion of medic…
CareFusion 303, Inc.CAFeb 5, 2025
Class IIOngoingZ-0990-2025
MICROVENTION INC. recalls Microvention
Sterility assurance; microcatheter inner packaging may contain incomplete seal.
MICROVENTION INC.CAJan 29, 2025
Class IIOngoingZ-0976-2025
CareFusion 303, Inc. recalls BD Pyxis Med 4000 Auxiliary (AUX)
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Sit…
CareFusion 303, Inc.CAJan 29, 2025
Class IIOngoingZ-0975-2025
CareFusion 303, Inc. recalls BD Pyxis Med ES Auxiliary (AUX)
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Sit…
CareFusion 303, Inc.CAJan 29, 2025
Class IIOngoingZ-0974-2025
CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 AUX
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Sit…
CareFusion 303, Inc.CAJan 29, 2025