Tyber Medical recalls specific anatomic lateral fibula plates due to reported surgical delays from locking screws passing through holes during use.
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices
Tyber Medical is recalling a specific type of surgical plate for right-sided use. This recall is due to reports that the locking screw can pass through the locking hole during surgery, causing delays.
The locking screw may pass through the locking hole during surgery, which can cause delays in the procedure. This issue has been reported in clinical use but does not typically cause serious injury.
Surgical patients and medical professionals who have the specific model of anatomic lateral fibula plate (6-hole, right side) with catalog number 770708062. Those at highest risk are patients undergoing orthopedic surgery with this device.
Check if your surgical plate is labeled 'Anatomic Lateral Fibula Plate, 6-hole, Right' with catalog number 770708062. Lot numbers 265783, 267847, 24036BU02, and 261289 are also affected.
Verify the product label for the specific model and catalog number to confirm if it is recalled.
The recall is due to reports that the locking screw can pass through the locking hole during surgery, causing delays in procedures.
No, but you should check if your product is recalled and contact Tyber Medical if you have the specific model with catalog number 770708062.
Check the product label for the specific model and catalog number. If it matches the recalled items, contact Tyber Medical for further instructions.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1212-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1212-2025 from Tyber Medical. 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.
