ZPLP — Class II medical device recall Z-1716-2024
Ongoing recall by Zimmer, Inc., reported 2024-05-08, distributed nationwide. Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The i
| Recall number | Z-1716-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2024-03-20 |
| Classified | 2024-04-30 |
| Reported by FDA | 2024-05-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CA, CH, CN, HK, IN, JP, KR, NZ, SG, TW |
| UPC / GTIN / UDI-DI | 00889024088573 |
| Lot numbers | 64370380, 64370382, 64423329, 64475643, 64661551, 64661552, 64745739, 64745742, 64745744, 64745745, 65635924, 65645147, 65755766, 65997131, 65997134, 66023658, 66166098, 66201200, 66233083, 66233084 |
| Model numbers | 47-2357-018-06 |
Product
ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-06
Reason for recall
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1716-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.