FDA Device recall Z-1722-2024
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Nonsterile- Indicated for temporary i…
- FDA Device
- Class II
- ongoing
- Published 2024-05-08
On 2024-05-08 the FDA classified a Class II recall of ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Nonsterile- Indicated for temporary i… by Zimmer, citing 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 sin….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1722-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-20 |
| Published | 2024-05-08 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Zimmer |
| Distribution | US |
Product
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-017-04
Reason
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
Identifiers
| code_info | GTIN: 00889024055865 Lot Numbers: 64370265 64370266 64370267 64370268 64370269 64370270 64370271 64370279 64370280 6437…GTIN: 00889024055865 Lot Numbers: 64370265 64370266 64370267 64370268 64370269 64370270 64370271 64370279 64370280 64370281 64370289 64370290 64370291 64370292 64370293 64370299 64370301 64370303 64370305 64370307 64475227 64475228 64475252 64475276 64475298 64475306 64475320 64475324 64475359 64475360 64475379 64475383 64528443 64528464 64528481 64528482 64528483 64528484 64528485 64528486 64528487 64528488 64528489 64528490 64528491 64528492 64528493 64528494 64528495 64552845 64552846 64552847 64552848 64552892 64552893 64552895 64552896 64552897 64552898 64552899 64552907 64552909 64552912 64552914 64552921 64553013 64553015 64553020 64553022 64553024 64553029 64553032 64553034 64553037 64563320 64563321 64563324 64563325 64563327 64572555 64572556 64572557 64572558 64572559 64572560 64572561 64572562 64572564 64572565 64572566 64572567 64572568 64572569 64572570 64572571 64572572 64572573 64572574 64572576 64572577 64572578 64572579 64572580 64572581 64572582 64572584 64588261 645 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1722-2024%22
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