Tyber Medical recalls specific A.L.P.S. mvX 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 certain A.L.P.S. mvX Anatomic Lateral Fibula Plates because locking screws may pass through the locking hole during surgery, causing delays. This could affect patients undergoing orthopedic procedures with these specific plates.
During surgical procedures, the locking screw may pass through the intended locking hole in the plate. This can cause delays in surgery as the issue must be corrected mid-procedure.
Orthopedic surgeons and patients using the recalled plates for tibia fracture fixation are most at risk. The recall applies to specific model numbers and lot numbers.
Check for the model number 770708102 on the plate. The recall includes lot numbers 265810, 260892, and 262559. These plates are intended for fixing tibia fractures.
Identify the model number (770708102) and lot numbers (265810, 260892, 262559) on the plate.
The recall is due to complaints that the locking screw may pass through the locking hole during surgery, causing delays.
The affected model number is 770708102 with lot numbers 265810, 260892, and 262559.
No immediate stop is required, but surgeons should check the model and lot numbers to confirm if the product is recalled.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1216-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1216-2025 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.
