Class IIOngoingZ-1621-2025
Stryker GmbH recalls Guide Wire with Ruler Tube 3x1000 mm DIA
The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
Stryker GmbHApr 23, 2025
Orthopedic Manual Surgical Instrument recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–5 of 5 recalls
Class IIOngoingZ-1620-2025
Stryker GmbH recalls Guide Wire with Ruler Tube 3x800 mm DIA
The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
Stryker GmbHApr 23, 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-1008-2025
Integrity Implants Inc. recalls Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Sof…
Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).
Integrity Implants Inc…FLJan 29, 2025