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
July 1, 2026FDABrand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral D…Z-2578-2026
July 1, 2026FDAOff-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110…Z-2531-2026
July 1, 2026FDAOff-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 1100…Z-2530-2026
July 1, 2026FDAOff-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Ca…Z-2528-2026
July 1, 2026FDAOff-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Cat…Z-2529-2026
July 1, 2026FDAOff-Axis Comprehensive Shoulder System Small, Augment, Off-Axis, Reamer Guide, Model/Cata…Z-2527-2026
May 6, 2026FDABrand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula …Z-1946-2026
December 31, 2025FDABrand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femo…Z-0970-2026
December 31, 2025FDABrand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femo…Z-0972-2026
December 31, 2025FDABrand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femo…Z-0968-2026
April 30, 2025FDAZimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Pr…Z-1648-2025
February 5, 2025FDANexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 …Z-1039-2025
November 13, 2024FDASaphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use in minimally inva…Z-0285-2025
August 7, 2024FDACPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis, used in Hip Arthroplast…Z-2450-2024
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 H…Z-1709-2024
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 16 H…Z-1721-2024
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 …Z-1722-2024
May 8, 2024FDAZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 6 Ho…Z-1716-2024
May 8, 2024FDAZPLP Distal Lateral Fibular Plate, Right, 8 Holes, 132 MM, Nonsterile- Indicated for temp…Z-1724-2024
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 16 …Z-1714-2024
May 8, 2024FDAZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Nonsterile- Indicated for tempor…Z-1726-2024
May 8, 2024FDAZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 12 …Z-1719-2024
May 8, 2024FDAZPLP Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Nonsterile- Indicated for tempo…Z-1727-2024
May 8, 2024FDAZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 10 H…Z-1718-2024
May 8, 2024FDAZPLP Distal Lateral Fibular Plate, Right, 10 Holes, 158 MM, Nonsterile- Indicated for tem…Z-1725-2024

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.
What was the most recent Zimmer, Inc. recall?
FDA recall Z-2578-2026, published July 1, 2026: Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description: Persona Revis…
Which agencies have handled Zimmer, Inc. recalls?
Zimmer, Inc. appears as the recalling firm in recalls from: FDA (397).

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