Vanguard Knee System Series-A Standard Patella sizes 31mm Item… — Class II medical device recall Z-0937-2019
Terminated recall by Zimmer Biomet, Inc., reported 2019-03-06, distributed in MN, VA. Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the impl
| Recall number | Z-0937-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2018-12-21 |
| Classified | 2019-02-23 |
| Reported by FDA | 2019-03-06 |
| Terminated | 2020-05-13 |
| Distributed | MN, VA |
| Countries outside the US | JP, KR, NZ |
| Quantity | 45 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00880304431317 |
| Lot numbers | 399960 |
| Model numbers | 184764 |
Product
Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764
Reason for recall
Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0937-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.