Zimmer recalls specific ZPLP distal lateral fibular plates due to thread form issues that may cause improper screw mating, leading to potential delays in surgery 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 for possible improper screw locking, which could delay surgery or require additional procedures. This affects surgeons using specific model numbers and lot numbers.
The locking screws may not properly engage with the plate due to a thread form issue. This could lead to the screws not locking correctly, potentially causing delays in surgery or requiring additional interventions to stabilize the fracture.
Surgeons who use the recalled Zimmer Periarticular Locking Plate System (ZPLP) distal lateral fibular plates for left leg fractures. The risk is primarily for medical professionals during surgical procedures.
Check if your plate has the model number 47-2357-018-08 and lot numbers 64568169, 64697763, 64697764, 65755769, 65782566, 65782567, or 66233085. These plates are used for temporary internal fixation of fractures.
Verify the model number 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 improper screw mating with the plate, potentially delaying surgery or requiring additional procedures.
The official recall notice does not specify a remedy, so contact Zimmer directly for guidance on next steps.
The recall addresses potential surgical delays or additional interventions, but does not indicate patient injury risks.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1717-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1717-2024 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.
