ASI 2 — Class II medical device recall Z-0517-2020
Terminated recall by Zimmer Biomet, Inc., reported 2019-12-04, distributed in AR, CA, CO, IN, KY, LA, MN, NJ…. The potential that the end of the shaft could fail to effectively mate with the broach with the Calcar Planar
| Recall number | Z-0517-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2019-08-06 |
| Classified | 2019-11-22 |
| Reported by FDA | 2019-12-04 |
| Terminated | 2020-08-24 |
| Distributed | AR, CA, CO, IN, KY, LA, MN, NJ, NY, OH, TX |
| Quantity | 73 |
| Lot numbers | 662870, 784060 |
| Model numbers | 110032331, 11032331, 662870, 784060 |
Product
ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
Reason for recall
The potential that the end of the shaft could fail to effectively mate with the broach with the Calcar Planar Shaft instrument, part number 110032331.
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-0517-2020. 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.