Zimmer, Inc.

Complete recall history across all FDA and CPSC categories — 437 total recalls

Zimmer, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (437)

FDA medical device enforcement actions by Zimmer, Inc.. Showing most recent 50.

Date Product Reason Class
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Dec 2, 2025 Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus An... Affected implants may have undersized distal diameter along length of the sha... Class II
Sep 26, 2025 Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm ... Zimmer Biomet is conducting a medical device recall for two (2) lots of the D... Class II
Sep 26, 2025 Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm ... Zimmer Biomet is conducting a medical device recall for two (2) lots of the D... Class II
Mar 24, 2025 Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, -3 Neck, Model Number 8... The associated product labeling does not adequately provide compatibility inf... Class II
Mar 24, 2025 Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Neck, Model Number 8... The associated product labeling does not adequately provide compatibility inf... Class II
Mar 24, 2025 Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +0 Neck, Model Num... The associated product labeling does not adequately provide compatibility inf... Class II
Mar 24, 2025 Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +3 Neck, Model Num... The associated product labeling does not adequately provide compatibility inf... Class II
Mar 24, 2025 Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 8... The associated product labeling does not adequately provide compatibility inf... Class II
Feb 27, 2025 NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-co... The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label ... Class II
Feb 12, 2025 Z1 Femoral Hip System, Product Number 611777612 There is a potential design issue with the Z1 Offset Stem Inserter leading to... Class II
Jan 6, 2025 NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C,D ... It was identified internally that two commingle events occurred where the met... Class II
Jan 6, 2025 NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F ... It was identified internally that two commingle events occurred where the met... Class II
Sep 17, 2024 Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use in mi... A Gen 5 tail piece was assembled to a Gen 4 Finished Device, resulting in a 0... Class II
Jul 2, 2024 CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis, used in Hip... Affected product has an increased risk of postoperative perisprosthetic femor... Class II
Mar 28, 2024 NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of ... Out of specification violation of devices that results in a gap existing with... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plat... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP Distal Lateral Fibular Plate, Right, 10 Holes, 158 MM, Nonsterile- Indic... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Nonsterile-Indicate... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Sterile- Indicated f... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Nonsterile-Indicat... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plat... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Nonsterile- Indicate... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Nonsterile- Indicat... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP Distal Lateral Fibular Plate, Right, 8 Holes, 132 MM, Nonsterile- Indica... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plat... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP Distal Lateral Fibular Plate, Left, 14 Holes, 210 MM, Sterile- Indicated... Thread form issue for the locking holes in that the locking screws may not pr... Class II
Mar 20, 2024 ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate... Thread form issue for the locking holes in that the locking screws may not pr... Class II

View all 437 device recalls →

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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