Orthopedic Salvage System — Class II medical device recall Z-0590-2019
Terminated recall by Zimmer Biomet, Inc., reported 2018-12-19, distributed in IN, MD, MO, MS, NM. Zimmer Biomet is conducting a lot specific medical device recall for two lots of the Orthopedic Salvage System
| Recall number | Z-0590-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2018-10-10 |
| Classified | 2018-12-07 |
| Reported by FDA | 2018-12-19 |
| Terminated | 2020-04-28 |
| Distributed | IN, MD, MO, MS, NM |
| Quantity | 3 total |
| Reason classes | labeling |
| Model numbers | 150394 |
Product
Orthopedic Salvage System (OSS) Porous Stem, Item No. 150394
Reason for recall
Zimmer Biomet is conducting a lot specific medical device recall for two lots of the Orthopedic Salvage System (OSS) and the Comprehensive Shoulder System. The investigation determined that the Mini Humeral Stem is potentially labeled as the Bowed IM Stem lot. The associated risk of this product issue is a potential extension of surgery <30 minutes if a replacement is readily available.
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-0590-2019. 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.