Coonrad/Morrey Total Elbow Humeral Assembly — Class II medical device recall Z-1000-2020
Terminated recall by Zimmer Biomet, Inc., reported 2020-02-12, distributed in CA, OH. The lot contained two outer pins instead of one outer and one inner pin.
| Recall number | Z-1000-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2019-12-12 |
| Classified | 2020-02-05 |
| Reported by FDA | 2020-02-12 |
| Terminated | 2021-01-13 |
| Distributed | CA, OH |
| Quantity | 3 |
| UPC / GTIN / UDI-DI | 00889024274006 |
| Lot numbers | 64481139 |
| Model numbers | 32-8105-027-04 |
Product
Coonrad/Morrey Total Elbow Humeral Assembly, Extra Small, 4-inch Length. Model No. 32-8105-027-04. UDI (01)00889024274006 (17)241031(10)64481139 The device is a Humeral component; elbow joint metal/polymer constrained cemented prosthesis.
Reason for recall
The lot contained two outer pins instead of one outer and one inner pin.
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-1000-2020. 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.