Zimmer recalls a specific fibular plate model due to thread form issues that may cause improper screw locking, potentially delaying surgery or requiring additional procedures. Affected units have a specific lot number and item number.
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 type of fibular plate used in surgery because its thread design might not lock properly with screws. This could lead to surgery delays or needing extra procedures if the plate doesn't stay securely in place.
The plate's locking holes have a thread form issue that might not securely engage with screws. If the screw doesn't lock properly, it could cause the plate to become loose during surgery, potentially requiring additional procedures or delaying the surgery.
Surgical patients who received the specific Zimmer Periarticular Locking Plate System model with lot number 66060712 are affected. Surgeons and medical teams using this exact model during procedures are most at risk.
Check for the item number 47-2357-017-10 and lot number 66060712 on the product packaging. This specific fibular plate is used in surgical procedures for temporary bone fixation.
Look for the item number 47-2357-017-10 and lot number 66060712 on the packaging to confirm if your product is affected.
The thread form issue may cause screws to not lock properly with the plate, potentially delaying surgery or requiring additional procedures.
Check the item number and lot number on the packaging to see if it's affected. If it is, contact Zimmer for further instructions.
The recall record does not specify a remedy, so no immediate fix is provided. Affected units should be checked and contacted by the manufacturer.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1712-2024 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1712-2024 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.
