Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSML — Class II medical device recall Z-1239-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-04-04. One lot of humeral stem implants do not include the humeral bushing components.
| Recall number | Z-1239-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2018-01-24 |
| Classified | 2018-03-28 |
| Reported by FDA | 2018-04-04 |
| Terminated | 2019-04-09 |
| Countries outside the US | CN, TW |
| Quantity | 9 |
| Lot numbers | 63694912 |
| Model numbers | 32-8105-027-04 |
Product
Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSML, Item Number: 32-8105-027-04 (UDI: (01)0088902427 4006(17)220731(10)63694912)
Reason for recall
One lot of humeral stem implants do not include the humeral bushing components.
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-1239-2018. 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.