Zimmer recalls specific ZPLP Distal Lateral Fibular Plates due to thread form issues that may cause improper screw locking, potentially delaying surgery or requiring 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 improper screw locking, which could delay surgery or require additional procedures. This affects surgeons and medical staff using these specific implants.
The locking screws may not properly engage with the plate due to a thread form issue. This can lead to the screw not locking correctly, which might delay surgery or require additional procedures to fix the problem.
Surgeons and medical staff who use Zimmer's ZPLP Distal Lateral Fibular Plates for temporary fracture fixation are most at risk. The recall applies to specific model numbers and lot numbers listed in the official notice.
Check for the model number ZPLP Distal Lateral Fibular Plate, Right, 8 Holes, 132 MM, Nonsterile. Look for lot numbers listed in the official recall notice (e.g., 64475412, 64475418, etc.).
Identify the model number and lot numbers from the product packaging or documentation to confirm if it is recalled.
Zimmer recalls these plates due to a thread form issue that may cause improper screw locking, potentially delaying surgery or requiring additional procedures.
The recall does not specify a remedy, so contact Zimmer directly to confirm if your specific model and lot number are affected.
The hazard may cause improper screw locking, which could delay surgery or require additional procedures, but the recall does not mention immediate injury risks.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1724-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1724-2024 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.
