ASI 2 — Class II medical device recall Z-0871-2020
Terminated recall by Zimmer Biomet, Inc., reported 2020-02-05, distributed nationwide. Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broac
| Recall number | Z-0871-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2019-12-19 |
| Classified | 2020-01-28 |
| Reported by FDA | 2020-02-05 |
| Terminated | 2020-08-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CN, NL |
| Quantity | 67 units |
| Lot numbers | 203240, 711160, 827310 |
Product
ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgical instrument
Reason for recall
Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach
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-0871-2020. 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.