Orthopedic Salvage System — Class II medical device recall Z-2236-2019
Terminated recall by Zimmer Biomet, Inc., reported 2019-08-21, distributed in AZ, CA, DC, GA, IL, KY, LA, MA…. Cleaning processes potentially being ineffective
| Recall number | Z-2236-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2019-07-02 |
| Classified | 2019-08-09 |
| Reported by FDA | 2019-08-21 |
| Terminated | 2021-09-10 |
| Distributed | AZ, CA, DC, GA, IL, KY, LA, MA, MD, MN, NC, NJ, NM, OH, OK, OR, SC, TX |
| Countries outside the US | JP, NL |
| Quantity | 19 |
| Model numbers | 151815 |
Product
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151815
Reason for recall
Cleaning processes potentially being ineffective
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-2236-2019. 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.