Tyber Medical recalls A.L.P.S. mvX Anatomic Lateral Fibula Plate 8H LT due to reported surgical delays from locking screws passing through holes during use. Affected models include 770708081 with specific lot numbers.
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 its A.L.P.S. mvX Anatomic Lateral Fibula Plate 8H LT model because locking screws have been reported to pass through the locking hole during surgery, causing delays. This could lead to complications if the device is used without proper fixation.
The locking screw may pass through the locking hole during surgery, causing the device to become unstable. This can lead to surgical delays as the procedure may need to be repeated or adjusted.
Surgical teams using the A.L.P.S. mvX Anatomic Lateral Fibula Plate 8H LT model for bone stabilization are affected. Patients undergoing orthopedic surgery with this specific device are at risk of delayed procedures.
Check for the model number 770708081 on the device. Lot numbers 265784, 24043BU01, and 261290 are associated with this recall. The product is intended for left-sided bone stabilization.
Verify the model number on the device; affected units have model 770708081.
Reach out to Tyber Medical for guidance on next steps if you have the recalled model.
The recall is due to complaints that the locking screw passes through the locking hole during surgery, causing delays.
The affected model number is 770708081 with lot numbers 265784, 24043BU01, and 261290.
The official recall does not specify a fix; affected users should contact Tyber Medical for guidance.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1213-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1213-2025 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.
