FDA Device recall Z-1000-2020
Coonrad/Morrey Total Elbow Humeral Assembly, Extra Small, 4-inch Length
- FDA Device
- Class II
- terminated
- Published 2020-02-12
On 2020-02-12 the FDA classified a Class II recall of Coonrad/Morrey Total Elbow Humeral Assembly, Extra Small, 4-inch Length by Zimmer Biomet, citing the lot contained two outer pins instead of one outer and one inner pin.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1000-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-12 |
| Published | 2020-02-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Zimmer Biomet |
| Distribution | CA, OH |
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
The lot contained two outer pins instead of one outer and one inner pin.
Identifiers
| code_info | Lot 64481139 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1000-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.