Zimmer recalls specific distal lateral fibular plates due to thread form issues that may cause improper screw mating, 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 a specific type of fibular plate used in surgery because the locking screws might not fit properly. This could lead to delays in surgery or the need for extra procedures if the plate doesn't hold securely.
The locking screws may not properly engage with the plate's threads, which can cause the screw to become loose or fail to lock. This might delay surgery or require additional procedures to fix the issue.
Surgical patients who have received the specific Zimmer Periarticular Locking Plate System distal lateral fibular plate (model 47-2357-017-08) are affected. Surgeons and medical staff using this product during procedures are most at risk.
Check if your plate has the model number 47-2357-017-08 and lot numbers 64811254, 64811255, or 65834885. This product was sold as a sterile surgical implant.
Verify your plate's model number and lot numbers to confirm if it is part of this recall.
Zimmer recalls this specific fibular plate due to thread form issues that may cause improper screw mating, potentially delaying surgery or requiring additional procedures.
Check your plate's model number and lot numbers to see if it is part of this recall. If it is, contact Zimmer for further instructions.
The recall indicates potential delays in surgery or additional procedures, but does not mention risks of serious injury to patients.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1711-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1711-2024 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.
