Zimmer recalls specific ZPLP Distal Lateral Fibular Plates due to thread form issues that may cause improper screw fixation, risking surgery delays or additional procedures.
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 certain distal lateral fibular plates for possible thread form issues that could lead to screws not locking properly. This might cause delays in surgery or require additional procedures if the plate fails to stay fixed.
The locking screws may not properly engage with the plate's threads, leading to the screw not being recognizable as locked. This could cause the plate to become loose during surgery, potentially requiring additional procedures or delaying the surgery.
Orthopedic surgeons and medical professionals who use Zimmer's ZPLP Distal Lateral Fibular Plates for temporary bone fixation are most at risk. Patients undergoing surgery with these specific plates could face complications.
Check for the product name 'ZPLP Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Nonsterile' with the listed lot numbers (64403506 to 66183916).
Verify the product name and lot numbers listed in the recall notice to confirm if your item is affected.
The recall is due to a thread form issue where locking screws may not properly mate with the plate, potentially causing fixation failure during surgery.
The official recall notice does not specify a remedy, so contact Zimmer directly for guidance.
The recall indicates potential for surgery delays or additional procedures, but does not mention serious injury risks in normal use.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1727-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1727-2024 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.
