Class IIOngoingZ-1511-2025
Cordis US Corp recalls Cordis
product mix-up; Vascular stent labeled as one size but contains a different size.
Cordis US CorpFLApr 9, 2025
Recalls: Employee error
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 25–32 of 32 recalls
Class IIOngoingZ-1510-2025
Cordis US Corp recalls Cordis
product mix-up; Vascular stent labeled as one size but contains a different size.
Cordis US CorpFLApr 9, 2025
Class IIOngoingZ-1503-2025
Fisher Diagnostics recalls Pacific Hemostasis Thromboplastin-D
The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.
Fisher DiagnosticsVAApr 9, 2025
Class IIOngoingZ-1502-2025
Fisher Diagnostics recalls Pacific Hemostasis Thromboplastin-D
The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.
Fisher DiagnosticsVAApr 9, 2025
Class IIOngoingZ-1330-2025
Cordis US Corp recalls Vista Brite Tip
Catheter manufactured at the incorrect length.
Cordis US CorpFLMar 19, 2025
Class IIOngoingZ-1315-2025
DePuy Mitek, Inc., A Johnson & Johnson Co. recalls COR Disposable Kit
Device is missing the pin in the graft loader component.
DePuy Mitek, Inc., a J…MAMar 19, 2025
Class IIOngoingZ-1314-2025
DePuy Mitek, Inc., A Johnson & Johnson Co. recalls COR Disposable Kit
Device is missing the pin in the graft loader component.
DePuy Mitek, Inc., a J…MAMar 19, 2025
Class IIOngoingZ-1232-2025
Physio-Control, Inc. recalls LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopu…
Incorrect keypad was incorrectly installed onto a defibrillator/monitor.
Physio-Control, Inc.WAMar 5, 2025