Vanguard 360 Revision System Posterior Augment With Bolt — Class II medical device recall Z-0723-2021
Terminated recall by Biomet, Inc., reported 2020-12-30, distributed nationwide. Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure
| Recall number | Z-0723-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2020-12-01 |
| Classified | 2020-12-23 |
| Reported by FDA | 2020-12-30 |
| Terminated | 2022-07-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | JP, KR, NL |
| Quantity | 21 units |
| UPC / GTIN / UDI-DI | 00880304482739 |
| Lot numbers | 098780 |
| Model numbers | 185422 |
Product
Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee arthroplasty Item Number: 185422
Reason for recall
Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure
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-0723-2021. 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.