Zimmer recalls specific distal lateral fibular plates due to thread form issues that may cause improper screw mating, potentially delaying surgery or requiring additional fixation.
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 that have a thread form issue. This could cause screws to not lock properly, leading to surgery delays or needing extra procedures.
The locking screws may not properly engage with the plate, making it hard for users to tell if the screw is locked correctly. This could delay surgery or require additional procedures to fix the problem.
Orthopedic surgeons and medical staff who use the recalled plates for temporary fracture fixation are most at risk. Patients receiving these plates during surgery are affected.
Check for the specific model: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Sterile. Look for lot numbers 65703586, 65703587, 66247618, or 66247619.
Verify the model number and lot numbers listed in the recall notice to confirm if your item is affected.
The locking screws may not properly mate with the plate, which could lead to surgery delays or requiring additional procedures.
The recall notice does not specify a remedy, so check the product details to see if it is affected.
Look for the model: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Sterile. Check lot numbers 65703586, 65703587, 66247618, or 66247619.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1710-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1710-2024 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.
