Drill — Class II medical device recall Z-1475-2019
Terminated recall by Zimmer GmbH, reported 2019-05-29, distributed in AL, AR, AZ, CA, CO, FL, GA, HI…. An investigation identified that the products were possibly manufactured from a different material than define
| Recall number | Z-1475-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer GmbH, Winterthur, N/A, Switzerland |
| Recall initiated | 2019-04-08 |
| Classified | 2019-05-23 |
| Reported by FDA | 2019-05-29 |
| Terminated | 2020-05-11 |
| Distributed | AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, WY |
| Model numbers | ST502015403 |
Product
Drill, cannulated, 4x150mm, AO, Item Number ST502015403
Reason for recall
An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
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-1475-2019. 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.