Zimmer, Inc. recalls
Every recall we track for Zimmer, Inc. — 71 in all, from 2022–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Zimmer, Inc. peaked in 2025 (28); 71 since 2017.
All FDA recall records for Zimmer, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 8 | 0 | 8 |
| 2023 | 0 | 0 | 4 | 0 | 4 |
| 2024 | 0 | 15 | 9 | 0 | 24 |
| 2025 | 0 | 5 | 23 | 0 | 28 |
| 2026 (to date) | 0 | 1 | 6 | 0 | 7 |
What to do if you have a recalled Zimmer, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Zimmer, Inc. recalls
20 shown- Lower riskMedical device
Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241
Zimmer recalls Off-Axis Comprehensive Shoulder System model 110040241 due to plastic guides catching during reaming, causing breakage. Five complaints reported.
ZimmerMay 20, 2026 - Lower riskMedical device
Zimmer, Inc. recalls Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog
Zimmer recalls Persona Revision Femoral Distal Augment model 42-5572-066-10 due to posterior augment found in distal package. Affected patients should contact Zimmer for details.
ZimmerMay 11, 2026 - Lower riskMedical device
Zimmer, Inc. recalls Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number:
Zimmer recalls 20-pack disposable mixing bowls with spatulas due to potential package seal failures that could compromise sterile barriers during surgery.
ZimmerMar 30, 2026 - Lower riskMedical device
Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that may cause fractures. Affected implants could lead to pain, surgery, or tissue damage. Check model numbers 815509420 and lot numbers 66717556 or 66884566.
ZimmerDec 2, 2025 - Lower riskMedical device
Zimmer, Inc. recalls Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 44 mm O.D., Size F, Bearing,
Zimmer Biomet recalls two lots of Dual Mobility Vivacit-E bearings due to size mixup between Size F and Size G implants. This mismatch could cause improper joint fit and complications during surgery.
ZimmerSep 26, 2025 - Lower riskMedical device
Zimmer, Inc. recalls Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Prosthesis, Hip,
Zimmer Biomet recalls ceramic hip prostheses with 22.2mm diameter heads that may not fit with certain stems, risking improper fit and injury. Affected units include specific model numbers and lots.
ZimmerMar 24, 2025 - Lower riskMedical device
Zimmer, Inc. recalls NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model
Zimmer recalls specific NexGen LPS Flex knee prostheses due to mismatched label compatibility statements. Affected units may not be safe for use with certain plates. Contact Zimmer for details.
ZimmerFeb 27, 2025 - Use cautionMedical device
Zimmer, Inc. recalls Z1 Femoral Hip System, Product Number 611777612
Zimmer recalls Z1 Femoral Hip System (Product #611777612) due to potential stem inserter fracturing. Affected units include specific lot numbers and UDI-DI codes. Contact Zimmer for details.
ZimmerFeb 12, 2025 - Lower riskMedical device
Zimmer, Inc. recalls NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10
Zimmer recalls specific NexGen LCCK Legacy Articular Surface models due to potential incorrect assembly of the metal support post, which could affect joint stability.
ZimmerJan 6, 2025 - Use cautionMedical device
Zimmer, Inc. recalls Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use in minimally invasive surgery allowing access
Zimmer recalls Saphena Medical Venapax XL endoscopic vessel harvesting systems due to potential endoscope slot misalignment causing surgical interference. Affected units have specific lot numbers and item codes.
ZimmerSep 17, 2024 - Use cautionMedical device
Zimmer, Inc. recalls CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis, used in Hip Arthroplasty; Item Numbers 00811400000
Zimmer recalls hip joint implants with increased risk of postoperative femur fracture. Affected models include specific item numbers for hip arthroplasty procedures.
ZimmerJul 2, 2024 - Lower riskMedical device
Zimmer, Inc. recalls NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.
Zimmer recalls NexGen CR-Flex Femoral Components (Size E and E-) due to a gap in metal bonding that could cause failure. Affected items have specific UDI codes listed in the recall.
ZimmerMar 28, 2024 - Use cautionMedical device
Zimmer, Inc. recalls ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Sterile- Indicated
Zimmer recalls specific left fibular plates for potential surgery delays due to improper screw locking. Affected items have unique lot numbers; contact Zimmer for details.
ZimmerMar 20, 2024 - Lower riskMedical device
Zimmer, Inc. recalls M/L Taper Hip Prosthesis Extended Offset, Reduced Neck Length, Size 4 (Item Number 00771100640) and Size 6 (Item Number
Zimmer recalls two hip implant models with incorrect size labeling. This mix-up could lead to improper fit if used, but no injuries reported. Affected units include specific item numbers and lot numbers.
ZimmerJul 26, 2023 - Lower riskMedical device
Zimmer, Inc. recalls Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral Femoral Plate 6 holes 159 mm Length-Indicated for temporary
Zimmer recalls certain Periarticular Locking Plates due to thread form issues that may cause screws to not lock properly, potentially leading to instability in bone fractures.
ZimmerJun 27, 2023 - Lower riskMedical device
Zimmer, Inc. recalls NexGen Precoat Stemmed Tibial Plate Size 5
Zimmer recalls NexGen Precoat Stemmed Tibial Plate Size 5 due to incorrect outer packaging labeling. No action needed as the hazard is a labeling error, not a safety issue.
ZimmerMay 19, 2023 - Lower riskMedical device
Zimmer, Inc. recalls CoCr Femoral Head, XS, 38/-8, Taper 12/14-Intended to be used as a modular head component for articulation in total hip
Zimmer recalls CoCr Femoral Head XS models due to potential reduced hip mobility. Affected units may not meet ISO 21535:2009 standards for range of motion. Contact Zimmer for details.
ZimmerFeb 27, 2023 - Lower riskMedical device
Zimmer, Inc. recalls Identity Shoulder System Resection Planer 35mm Resection Planer
Zimmer recalls Identity Shoulder System Resection Planer 35mm models that are unusable during sawbones shoulder training. Affected units have specific lot numbers and item numbers.
ZimmerDec 7, 2022 - Lower riskMedical device
Zimmer, Inc. recalls NexGen Option Stemmed Tibial Component Size 7, Item Number 00-5986-057-01
Zimmer recalls NexGen Stemmed Tibial Component Size 7 due to higher revision rates when used with specific LPS Flex femoral components in UK joint registry data. Affected patients should contact Zimmer for guidance.
ZimmerDec 6, 2022 - Lower riskMedical device
Zimmer, Inc. recalls G7 Acetabular System, Acetabular Shell, Item numbers Item Numbers: 010000663 (52 MM E), 010000667 (60 MM G). used in
Zimmer recalls G7 Acetabular System (item numbers 010000663 and 010000667) due to thin package corners that may crack during shipping, risking surgery extension or infection.
ZimmerAug 25, 2022
Zimmer, Inc. recall questions
How many recalls has Zimmer, Inc. had?
71 recalls from Zimmer, Inc. are on record with U.S. safety agencies, from 2022–2026.
What is the most recent Zimmer, Inc. recall?
Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241, dated May 20, 2026. Every Zimmer, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Zimmer, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Zimmer, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.