Class II — Zimmer, Inc.
| Recalling firm | ZIMMER, INC. |
|---|---|
| Registered facility | View this company's 10 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Device outer packaging was incorrectly labeled. |
| Product | NexGen Precoat Stemmed Tibial Plate Size 5 |
| Quantity | N/A |
| Distribution | International distribution in the country of India. |
| Initiated | 2023-05-19 |
| Classified | 2023-07-05 |
| Terminated | 2026-05-29 |
| Recall number | Z-2092-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Zimmer, Inc. (Z-2092-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92531/
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