Orthopedic Salvage System — Class II medical device recall Z-1522-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-05-02, distributed in CT, FL, GA, IN, MA, MI, NY, TX. There is a potential dry blast irregularity on the locking collar screws packaged with the locking collar.
| Recall number | Z-1522-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2018-04-03 |
| Classified | 2018-04-25 |
| Reported by FDA | 2018-05-02 |
| Terminated | 2018-07-02 |
| Distributed | CT, FL, GA, IN, MA, MI, NY, TX |
| Countries outside the US | MY, NL |
| Lot numbers | 333020, 360610 |
| Model numbers | CP260600 |
Product
Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar, Model Number CP260600 Product Usage: The replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee.
Reason for recall
There is a potential dry blast irregularity on the locking collar screws packaged with the locking collar.
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-1522-2018. 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.