FDA Device recall Z-1723-2024
ZPLP Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteo…
- FDA Device
- Class II
- ongoing
- Published 2024-05-08
On 2024-05-08 the FDA classified a Class II recall of ZPLP Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteo… 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-1723-2024 |
| 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 Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-017-06
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: 00889024055872 Lot Numbers: Lot Number 63579608 63579611 63579634 64403617 64403618 64403619 64403624 64403625 64…GTIN: 00889024055872 Lot Numbers: Lot Number 63579608 63579611 63579634 64403617 64403618 64403619 64403624 64403625 64403626 64403627 64403628 64403629 64403630 64403631 64403632 64403633 64403634 64423729 64423730 64423731 64423732 64423733 64423734 64423735 64423736 64423737 64423738 64423739 64423740 64423741 64423742 64475394 64475399 64528496 64528497 64528498 64528499 64528501 64528502 64528503 64528504 64528505 64528506 64544896 64544898 64544899 64544901 64544902 64544903 64544904 64544905 64544907 64544908 64544909 64544912 64544913 64544915 64544916 64544917 64544919 64544920 64544921 64544922 64544923 64544924 64544925 64544926 64544928 64544929 64572585 64572586 64572587 64572588 64572589 64572590 64572591 64588269 64588270 64588271 64588272 64588273 64588274 64588275 64588276 64588277 64588278 64588279 64588280 64588281 64610599 64610602 64610604 64610605 64610606 64610607 64610608 64610609 64610610 64610611 64610612 64648204 64648205 64648206 64648207 64648208 64648209 6 |
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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-1723-2024%22
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