Zimmer recalls specific 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 because the locking screws might not properly attach to the plate. This could cause delays in surgery or require additional procedures if the screw doesn't lock correctly.
The locking screws may not properly mate with the plate's threads, making it hard for the user to recognize if the screw is locked correctly. This could lead to delays in surgery or the need for additional procedures if the plate doesn't stay fixed properly.
Orthopedic surgeons and medical professionals who use Zimmer's ZPLP distal lateral fibular plates for temporary fracture fixation. Patients who have received these plates are not directly affected by the recall.
Check for the product name 'Zimmer Periarticular Locking Plate System' with the specific model: Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Nonsterile. Lot numbers listed in the recall include many numbers starting with 64370265 through 66240999.
Identify the product by checking the item number (00-2357-017-04) or lot numbers listed in the recall.
No, the recall does not require immediate discontinuation. The hazard is a potential risk during surgery, not a safety issue for end users.
The official recall notice does not specify a remedy, so no action is required beyond checking the product details.
The recall states the issue may lead to delays in surgery or additional procedures, but it does not mention patient injuries.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1722-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1722-2024 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.
