FDA Device recall Z-2092-2023
NexGen Precoat Stemmed Tibial Plate Size 5
- FDA Device
- Class II
- terminated
- Published 2023-07-12
On 2023-07-12 the FDA classified a Class II recall of NexGen Precoat Stemmed Tibial Plate Size 5 by Zimmer, citing device outer packaging was incorrectly labeled.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2092-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2023-05-19 |
| Published | 2023-07-12 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Zimmer |
| Distribution | n/a |
Product
NexGen Precoat Stemmed Tibial Plate Size 5
Reason
Device outer packaging was incorrectly labeled.
Identifiers
| code_info | Model No. 00598004701; UDI No./Lot. No.: (01)00889024217607(17)321228(10)J7418537/J7418537 and (01)00889024217607(17)321228(10)J7418542/J7418542. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2092-2023%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.