Zimmer Recalls
550 recalls on record · September 5, 1978 to July 1, 2026 · Medical Devices, Vehicles
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 3, 2014Medical DevicesFDA
Zimmer, Inc. recalls Endo & Unipolar Femoral Heads: ENDO FEMORAL HEAD 43MM DIA, ENDO FEMORAL HEAD 53MM DIA, ENDO FEMORAL HEAD 47MM DIA, ENDO
Hazard: Zimmer is recalling sterile-packaged implants and instruments packaged in six different package configurations due to packaging design verification test failures. Specifically, multiple test samples from each of the six configurations failed simulated distribution and shipping testing when the devices either breached inner or outer package trays or seal integrity was lost.
September 3, 2014Medical DevicesFDA
Zimmer, Inc. recalls Endo & Unipolar Femoral Heads: ENDO FEMORAL HEAD 41MM DIA ENDO FEMORAL HEAD 42MM DIA ENDO FEMORAL HEAD 43MM DIA ENDO
Hazard: Zimmer is recalling sterile-packaged implants and instruments packaged in six different package configurations due to packaging design verification test failures. Specifically, multiple test samples from each of the six configurations failed simulated distribution and shipping testing when the devices either breached inner or outer package trays or seal integrity was lost.
September 3, 2014Medical DevicesFDA
Zimmer, Inc. recalls Knee Instrument Fixation Screws: 48MM HEADED SCREW 48MM HEADLESS SCREW MIS HEADED SCREW, 48MM MIS HEADLESS SCREW, 4
Hazard: Zimmer is recalling sterile-packaged implants and instruments packaged in six different package configurations due to packaging design verification test failures. Specifically, multiple test samples from each of the six configurations failed simulated distribution and shipping testing when the devices either breached inner or outer package trays or seal integrity was lost.
September 3, 2014Medical DevicesFDA
Zimmer, Inc. recalls Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral Trochlea Component, Precoat, Size 4, Left. Kn
Hazard: Internal review found that five (5) PFJ implant forgings were identified as have forged laps during receiving inspection process for raw material. These five forgings were not segregated and were subsequently issued to final manufacturing under Part 00-5926-014-01; lot 62455332. A forged lap is a defect that forms when metal folds over itself during forging.
September 3, 2014Medical DevicesFDA
Zimmer, Inc. recalls Zimmer PERSONA Distal Valgus Alignment Guide, Nonsterile. orthopedic surgical instrument. The device sets the prope
Hazard: Persona Distal Valgus Alignment guide collet locks are seizing in the 'unlocked' position.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls Persona (TM) The Personalized Knee System CPS Tibial Articular Surface Provisional Top Nonsterile TASP MLC L 3-5 CD
Hazard: Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). This is a retrospective recall which covers Zimmer's corrective actions taken earlier this year concerning the TASPs.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls Persona (TM) The Personalized Knee System Tibial Articular Surface Provisional Bottom Nonsterile PSN A/S PROV L CD B
Hazard: Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). This is a retrospective recall which covers Zimmer's corrective actions taken earlier this year concerning the TASPs.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls Persona (TM) The Personalized Knee System UC Tibial Articular Surface Provisional Top Nonsterile TASP UC L 3-7 CD TO
Hazard: Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). This is a retrospective recall which covers Zimmer's corrective actions taken earlier this year concerning the TASPs.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls Persona (TM) The Personalized Knee System CR Tibial Articular Surface Provisional Top Nonsterile TASP CR L 3-9 CD
Hazard: Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). This is a retrospective recall which covers Zimmer's corrective actions taken earlier this year concerning the TASPs.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls Persona (TM) The Personalized Knee System Tibial Articular Surface Provisional Bottom Nonsterile TASP L CD BOTTOM,
Hazard: Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). This is a retrospective recall which covers Zimmer's corrective actions taken earlier this year concerning the TASPs.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls Persona (TM) The Personalized Knee System PS Tibial Articular Surface Provisional Top Nonsterile TASP PS L 3-5 CD
Hazard: Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). This is a retrospective recall which covers Zimmer's corrective actions taken earlier this year concerning the TASPs.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls PERSONA (TM) The Personalized Knee System Tibial General Instrument Tray, non-sterile The intended use of the sterili
Hazard: The firm discovered that the current Personal Tibial/General Fixed Bracket Trays may not have the specific geometry to accommodate the tibial drill and stop guide with proper position/orientation. The drill bracket and drill guide are not the correct geometry to allow for a proper fit in the Persona Fixed Case Kit which could lead to improper sterilization of the tibial drill and stop guide.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls PERSONA (TM) The Personalized Knee System Tibial General Instrument Tray, non-sterile The intended use of the sterili
Hazard: The firm discovered that the current Personal Tibial/General Fixed Bracket Trays may not have the specific geometry to accommodate the tibial drill and stop guide with proper position/orientation. The drill bracket and drill guide are not the correct geometry to allow for a proper fit in the Persona Fixed Case Kit which could lead to improper sterilization of the tibial drill and stop guide.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls 4.0 mm Cancellous Screw, Partially Threaded Sterile Zimmer
Hazard: Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls 4.5 mm Malleolar Screw Sterile zimmer
Hazard: Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls 6.5 mm Cancellous Screw Fully Threaded Sterile zimmer
Hazard: Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls 6.5 mm Cancellous Screw 32 mm Thread Length Sterile zimmer
Hazard: Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls 6.5 mm Cancellous Screw 16 mm Thread Length Sterile zimmer
Hazard: Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls 6.5 mm Cancellous Screw Fully Threaded Sterile zimmer
Hazard: Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw Sterile zimmer
Hazard: Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
August 27, 2014Medical DevicesFDA
Zimmer, Inc. recalls Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer
Hazard: Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
August 20, 2014Medical DevicesFDA
Zimmer, Inc. recalls 23.5 Deg Rasp Handle Assy- RIGHT Nonsterile
Hazard: The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
August 20, 2014Medical DevicesFDA
Zimmer, Inc. recalls 23.5 Deg Rasp Handle Assy- LEFT Nonsterile
Hazard: The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
August 20, 2014Medical DevicesFDA
Zimmer, Inc. recalls VER2 HANDLE, PIN REWORK, RT Nonsterile
Hazard: The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
August 20, 2014Medical DevicesFDA
Zimmer, Inc. recalls VER2 HANDLE, PIN REWORK, LT Nonsterile
Hazard: The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
August 20, 2014Medical DevicesFDA
Zimmer, Inc. recalls Double Offset Rasp Handle, Right Hand A/S Rasp Handle (Right)
Hazard: The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
August 20, 2014Medical DevicesFDA
Zimmer, Inc. recalls Double Offset Rasp Handle, Left Hand A/S Rasp Handle (Left)
Hazard: The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
August 20, 2014Medical DevicesFDA
Zimmer, Inc. recalls VER2 D8L OFFSET RASP HANDLE, RT Nonsterile
Hazard: The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
August 20, 2014Medical DevicesFDA
Zimmer, Inc. recalls VER2 DBL OFFSET RASP HANDLE, LT Nonsterile
Hazard: The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
August 20, 2014Medical DevicesFDA
Zimmer, Inc. recalls Vl DBL OFFST WI LRG STPL, RT Nonsterile
Hazard: The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.