Zimmer recalls certain ZPLP Distal Lateral Fibular Plates due to thread form issues that may cause improper screw fixation, risking surgery delays or loss of stability.
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
Zimmer is recalling specific left fibular plates that have a thread form issue. This could cause screws to not lock properly, potentially delaying surgery or requiring additional procedures.
The locking screws may not properly mate with the plate due to a thread form issue. This can lead to screws not locking correctly, which might cause surgery delays or the need for additional procedures to stabilize the fracture.
Orthopedic surgeons and medical professionals who use Zimmer's ZPLP Distal Lateral Fibular Plates for temporary fracture fixation. The risk is primarily for those using the specific model numbers listed in the recall.
Check for the model name 'ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Nonsterile' with the specific lot numbers listed in the recall. The item number is 00-2357-018-04.
Verify the item number (00-2357-018-04) and lot numbers listed in the recall to confirm if your plate is affected.
The recall is for medical devices used in surgery. If you have the specific model numbers listed, contact Zimmer directly to discuss potential impacts on your procedure.
Check the item number (00-2357-018-04) and lot numbers provided in the recall notice to see if your plate matches.
The recall does not specify a remedy, so contact Zimmer directly for guidance on next steps.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1726-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1726-2024 from Zimmer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
