Zimmer, Inc.: 397 recalls on record

Recalls filed with 1 agency: FDA (397).

First recall on record: July 4, 2012. Most recent: July 1, 2026.

Risk classification: Class I: 1 · Class II: 396

Most recent recalls

DateAgencyProduct
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 8 Ho…Z-1717-2024
May 8, 2024FDAZPLP Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Nonsterile- Indicated for temp…Z-1723-2024
May 8, 2024FDAZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Sterile- Indicated for temporary…Z-1715-2024
May 8, 2024FDAZPLP Distal Lateral Fibular Plate, Left, 14 Holes, 210 MM, Sterile- Indicated for tempora…Z-1720-2024
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 8 H…Z-1711-2024
May 8, 2024FDAZPLP Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Nonsterile-Indicated for tempo…Z-1729-2024
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 6 …Z-1710-2024
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 10 …Z-1712-2024
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 …Z-1713-2024
May 8, 2024FDAZPLP Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Nonsterile-Indicated for tempor…Z-1728-2024
May 1, 2024FDANexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen C…Z-1608-2024
October 12, 2022FDAG7 Acetabular System, Acetabular Shell, Item numbers Item Numbers: 010000663 (52 MM E), 0…Z-0007-2023
October 14, 2015FDAZimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are…Z-0027-2016
October 7, 2015FDAZimmer Guide Wires for orthopedic procedures.Z-2820-2015
July 22, 2015FDAZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.Z-2060-2015
December 31, 2014FDAPersona Cemented Tibial Broach Inserter/Extractor. The Persona Cemented Tibial Broach …Z-0853-2015
December 17, 2014FDAZimmer Title 2 Bone Screw Remover Instrument, Part Number ET1093-01 Rx Only, Non-Sterile.…Z-0574-2015
December 3, 2014FDATrabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in …Z-0423-2015
December 3, 2014FDATrabecular Metal Tibial Impactor Replacement Pads. Product Usage: TM Tibial Impactor …Z-0424-2015
November 19, 2014FDAPersona Stemmed 5 Degree Cemented Tibia Product Usage: This device is indicated for…Z-0198-2015
October 29, 2014FDAContinuum Acetabular System Trabecular Metal Shell with Multi Holes, Porous 68mm, Prosthe…Z-0094-2015
October 29, 2014FDAThe Persona Tibial Articular Surface Inserter is a sterilizable instrument intended for …Z-0123-2015
October 8, 2014FDAPersona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Ster…Z-2737-2014
September 10, 2014FDAPERSONA The Personalized Knee System CR Tibial Articular Surface Provisional with the fol…Z-2577-2014
September 10, 2014FDAPERSONA The Personalized Knee System Constrained Tibial Articular Surface Provisional BOT…Z-2575-2014

Questions about this company

How many recalls does Zimmer, Inc. have?
Recalert has 397 U.S. recalls on record for Zimmer, Inc., published between July 4, 2012 and July 1, 2026.
Which agencies have handled Zimmer, Inc. recalls?
Zimmer, Inc. appears as the recalling firm in recalls from: FDA (397).

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