Drug recall
Coonrad/Morrey Total Elbow Humeral Assembly, Extra Small, 4-inch Length. Model No. 32-8105-027-04. UDI…
FDA recall event 84636 · Class II · Zimmer Biomet, Inc.
Key facts
| Event ID | 84636 |
|---|---|
| Recall numbers | Z-1000-2020 |
| Recalling firm | Zimmer Biomet, Inc. |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The lot contained two outer pins instead of one outer and one inner pin. |
| Initiation date | Dec 12, 2019 |
| Report date | Feb 12, 2020 |
| Termination date | Jan 13, 2021 |
| City | Warsaw |
| State | IN |
| Country | United States |
| FEI number | 1000220733 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: