The 2nd Assist Knee Positioner — Class II medical device recall Z-0803-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-03-07. Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential
| Recall number | Z-0803-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2017-09-07 |
| Classified | 2018-02-28 |
| Reported by FDA | 2018-03-07 |
| Terminated | 2018-08-23 |
| Quantity | 38,879 units |
| Reason classes | sterility |
| Model numbers | 740026 |
Product
The 2nd Assist Knee Positioner
Reason for recall
Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.