FDA Device recall Z-2198-2017
Reusable instruments in the Knee, Hip, Trauma, and Extremities segments
- FDA Device
- Class II
- terminated
- Published 2017-06-07
On 2017-06-07 the FDA classified a Class II recall of Reusable instruments in the Knee, Hip, Trauma, and Extremities segments by Zimmer Biomet, citing durability characteristics of reusable instruments were not established.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2198-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-05-08 |
| Published | 2017-06-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | US |
Product
Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
Reason
Durability characteristics of reusable instruments were not established
Identifiers
| code_info | All lots in distribution prior to 5/8/17 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2198-2017%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.