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 can pass through the locking hole during surgery, causing delays. This risk affects orthopedic surgeries where these plates are used to fix fractures.
During surgery, the locking screw can pass through the locking hole in the plate, which may cause surgical delays. This issue has been reported in clinical use but does not typically cause serious injury.
Orthopedic surgeons and medical facilities using the recalled plates for fracture fixation are most at risk. Patients undergoing surgery with these specific plates may experience delays.
Check for the model number 77070802, lot numbers 265785, 24036BU01, or 261291 on the plate. The product is indicated for use in fixing fractures of the distal tibia.
Identify the model number (77070802) and lot numbers (265785, 24036BU01, 261291) on the plate to confirm if it is recalled.
The recall is due to complaints that the locking screw can pass through the locking hole during surgery, causing reported delays in procedures.
Check for the model number 77070802 and lot numbers 265785, 24036BU01, or 261291 on the plate.
The recall does not require immediate discontinuation; surgeons should check product details to confirm if it is recalled before continuing use.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1214-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1214-2025 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.
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.
