Zimmer recalls specific ZPLP distal lateral fibular plates due to thread form issues that may cause improper screw mating, leading to surgery delays or loss of 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 for possible thread form issues that could cause screws to not lock properly. This might delay surgery or require additional procedures if the plate doesn't hold securely.
The locking screws may not properly engage with the plate's threads, making it hard for users to tell if the screw is locked correctly. This could cause the plate to become loose during surgery, requiring extra steps or delaying the procedure.
Surgical patients and medical professionals using Zimmer's ZPLP distal lateral fibular plates with specific lot numbers. Those undergoing orthopedic surgery are most at risk.
Check the product label for lot numbers: 65620069, 65635922, 65635923, 65674071, 65674072, 66010704, 66166096, or 66216633. These plates are part of the Zimmer Periarticular Locking Plate System.
Look for lot numbers on the plate: 65620069, 65635922, 65635923, 65674071, 65674072, 66010704, 66166096, or 66216633.
The locking screws may not properly mate with the plate's threads, which could cause the plate to become loose during surgery, requiring additional procedures or delaying the surgery.
Check the product label for lot numbers. If it matches the listed numbers, contact Zimmer for further instructions.
The recall states that improper screw mating could lead to surgery delays or loss of fixation, but it does not mention a risk of serious injury 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-1709-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1709-2024 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.
