FDA Device recall Z-1208-2015
Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 010000589 Lot: 527400
- FDA Device
- Class II
- terminated
- Published 2015-03-04
On 2015-03-04 the FDA classified a Class II recall of Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 010000589 Lot: 527400 by Biomet, citing the taper adaptor is missing from the packaging, which may result in a delay in surgery greater than 30 minutes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1208-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-07 |
| Published | 2015-03-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Biomet |
| Distribution | AL, FL, NY, TX |
Product
Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 010000589 Lot: 527400
Reason
The taper adaptor is missing from the packaging, which may result in a delay in surgery greater than 30 minutes.
Identifiers
| code_info | Part Number: 010000589 Lot: 527400 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1208-2015%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.