Zimmer recalls specific 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 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 cause surgery to be delayed or require additional procedures.
Orthopedic surgeons and medical staff using the recalled plates during surgery. Patients receiving these plates are at risk if the issue causes delays or additional procedures.
Check for the model name 'ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 Holes, 184 MM, Sterile'. Lot numbers 64475610, 65038408, 65038409, 65209412, or 65209413.
Verify the model name and lot numbers listed in the recall notice to confirm if your plate is affected.
The recall is due to a thread form issue that may cause screws to not lock properly with the plate, potentially delaying surgery or requiring additional procedures.
The recall notice does not specify a remedy, so check the product details to confirm if your plate is affected and contact Zimmer for further instructions.
The recall indicates a risk of surgery delays or additional procedures, but the hazard does not involve immediate injury or death.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1713-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1713-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
