Zimmer recalls
Zimmer has 539 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 1 Jul 2026. 72 are still ongoing. 26 were reported in the last 12 months. The most frequent reason is sterility.
Total recalls539since 2012
Last 12 months26reported
Class I20% of total
Ongoing72latest 1 Jul 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 2 0%Class II 537 100%Class III 0 0%
Why zimmer is recalled
Product types
By year
Ongoing zimmer recalls
72 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Off-Axis Comprehensive Shoulder System, Large, Augment recalled | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | Off-Axis Comprehensive Shoulder System Small, Augment recalled by Zimmer | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide recalled | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment recalled | Zimmer | Foreign Material | IN |
| Device | CLASS II | Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide recalled | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | Off-Axis Comprehensive Shoulder System, Medium, Augment recalled | Zimmer | Foreign Material | Nationwide |
All zimmer recalls, newest first
539 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.