Tyber Medical recalls A.L.P.S. mvX Medial Tibia plates due to reported surgical delays from locking screws passing through holes during use. Affected models include specific lot numbers and catalog codes.
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 Medial Tibia plates because locking screws can pass through the locking hole during surgery, causing delays. This risk affects patients who have received these plates for tibia fractures.
During surgery, the locking screw can pass through the locking hole, causing the plate to become unstable. This has led to reported surgical delays as the procedure must be stopped and corrected.
Patients who received the recalled A.L.P.S. mvX Medial Tibia plates for tibia fractures are most at risk. Healthcare providers using these plates during surgery may also be affected.
Check for the model number 770715061, lot numbers 265790, 263514, 24055DF05, or 24056DF01 on the plate. These specific plates were sold for tibia fracture fixation.
Look for the model number 770715061 and lot numbers 265790, 263514, 24055DF05, or 24056DF01 on the plate.
The recall is due to complaints that the locking screw passes through the locking hole during surgery, causing delays.
The official recall notice does not specify a remedy, so contact Tyber Medical for further instructions.
Affected models include the A.L.P.S. mvX Medial Tibia plate with model number 770715061 and lot numbers 265790, 263514, 24055DF05, or 24056DF01.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1219-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1219-2025 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.
