FDA Device recall Z-0871-2020
ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgi…
- FDA Device
- Class II
- terminated
- Published 2020-02-05
On 2020-02-05 the FDA classified a Class II recall of ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgi… by Zimmer Biomet, citing potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0871-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-19 |
| Published | 2020-02-05 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Zimmer Biomet |
| Distribution | US |
Product
ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgical instrument
Reason
Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach
Identifiers
| code_info | Lot Numbers: 827310, 711160, 203240 |
|---|
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-0871-2020%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.