Zimmer GmbH recalls
Every recall we track for Zimmer GmbH — 85 in all, from 2018–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Zimmer GmbH peaked in 2019 (77); 85 since 2017.
All FDA recall records for Zimmer GmbH 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 | 4 | 0 | 4 |
| 2019 | 0 | 0 | 76 | 1 | 77 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 2 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 2 | 0 | 2 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Zimmer GmbH 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 GmbH recalls
7 shown- Lower riskMedical device
Zimmer GmbH recalls Biolox Option Taper Sleeve, Type 1 Taper, -6mm Neck - Indicated for use in total hip replacement with cemented or
Zimmer recalls Biolox Option Taper Sleeves due to mislabeled packaging. The outer box lists a standard neck sleeve but contains a -6mm neck sleeve. This mismatch could lead to improper surgical use.
ZimmerAug 8, 2024 - UnratedMedical device
Zimmer GmbH recalls Zimmer Natural Nail -ZNN Cephalomedullary Short Nail 11.5 mm X 21.5 cm 125 CCD Left Ti-6Al-4V Alloy- intended for
Zimmer recalls specific natural nail implants due to potential angle mismatch causing improper bone fixation. Affected items have unique identifiers; contact Zimmer for details.
ZimmerMay 7, 2021 - Lower riskMedical device
Zimmer GmbH recalls Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500 orthopedic implant - Product Usage: The Sidus
Zimmer recalls Sidus Stem-Free Shoulder Humeral Head 50-18 implants due to incorrect labeling showing size 50-18 when actual size is 40-14. This mismatch could lead to improper surgical fitting.
ZimmerAug 21, 2019 - Lower riskMedical device
Zimmer GmbH recalls V-TEK", IVP step drill 2.5-3.9x124mm, 16mm stop, contra-angle, Item Number 502015637
Zimmer recalls V-TEK IVP step drills with "Normed" marking due to possible material mismatch in specifications. Affected items may not meet safety standards.
ZimmerApr 8, 2019 - Lower riskMedical device
Zimmer GmbH recalls Avenir¿ Muller Stem Standard, uncemented HA, 1, Taper 12/14 Item Number: 01.06010.001 - Product Usage: Avenir@ Muller
Zimmer recalls Avenir Muller Stem Standard size 1 due to mislabeling in packaging. The stem inside packaging is actually size 2, which could lead to improper fit during hip surgery.
ZimmerOct 31, 2018 - Lower riskMedical device
Zimmer GmbH recalls Normed Charcot Osteotome Chisel (Various sizes)
Zimmer recalls certain osteotome chisels that may not disinfect or sterilize properly due to a handle gap. Affected models include 26.08.506-910. No US distribution.
ZimmerMar 15, 2018 - Lower riskMedical device
Zimmer GmbH recalls Avenir Muller Stem; Item Number: 01.06010.104, Lot Number: 2905496, UDI: (01)00889024479500 (17)220430 (10)2905496
Zimmer recalls Avenir Muller Stem (Lot 2905496) due to potential mismatch between product in package and outer label. Consumers should check labels and contact Zimmer for details.
ZimmerFeb 28, 2018
Zimmer GmbH recall questions
How many recalls has Zimmer GmbH had?
85 recalls from Zimmer GmbH are on record with U.S. safety agencies, from 2018–2024.
What is the most recent Zimmer GmbH recall?
Zimmer GmbH recalls Biolox Option Taper Sleeve, Type 1 Taper, -6mm Neck - Indicated for use in total hip replacement with cemented or, dated Aug 8, 2024. Every Zimmer GmbH recall is listed on this page, newest first.
What should I do if I have a recalled Zimmer GmbH 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 GmbH 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.