Zimmer recalls specific left 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 a specific left fibular plate model because its locking screws might not fit properly. This could lead to surgery delays or the need for extra procedures if the plate doesn't stay securely in place.
The locking screws may not properly engage with the plate's holes, making it hard for users to tell if the screw is locked. This could cause the plate to become loose during surgery, requiring additional procedures or delaying treatment.
Orthopedic surgeons and medical staff who use the recalled Zimmer Periarticular Locking Plate System for left fibular fractures. Patients undergoing surgery with this specific plate are at risk if the screws don't lock correctly.
Check if your plate has the model name 'ZPLP (Zimmer Periarticular Locking Plate System)', is left-sided, has 12 holes, 184 mm length, and sterile packaging. Lot numbers 64381071 through 65233125 are affected.
Verify the model, size, and lot number against the list provided in the recall notice to confirm if your plate is affected.
The locking screws may not properly engage with the plate's holes, which could lead to surgery delays or additional procedures if the plate becomes loose.
Check the model, size, and lot number to see if it's in the recall list. If affected, contact Zimmer for further instructions.
The recall indicates potential delays in surgery or extra procedures, but the hazard does not describe 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-1719-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1719-2024 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.
