Zimmer recalls specific left fibular plates due to thread form issues that could lead to 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 a specific left fibular plate model because its locking screws might not fit properly, which could delay surgery or require extra procedures. This affects surgeons and medical staff using the product.
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 cause surgery delays or require additional procedures if the plate isn't fixed properly.
Surgeons and medical staff who use the recalled Zimmer Periarticular Locking Plate System for left fibular plates are most at risk. The recall impacts specific model numbers and lot numbers.
Check for the product name 'Zimmer Periarticular Locking Plate System' with the model 'Distal Lateral Fibular Plate, Left, 16 Holes, 236 MM, Sterile'. Look for lot numbers 64464711 or 66010706.
Verify the product model and lot numbers to confirm if it's affected.
The locking screws may not properly mate with the plate, which could cause surgery delays or require additional procedures.
The recall record does not specify a remedy, so check the product details to confirm if it's affected.
Lot numbers 64464711 and 66010706 are affected.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1721-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1721-2024 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.
