Tyber Medical recalls A.L.P.S. mvX Medial Tibia Plates with 10 holes for left tibia fractures 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.L.P.S. mvX Medial Tibia Plates for left tibia fractures. The recall is due to reports of locking screws passing through the locking hole during surgery, causing delays.
The locking screw may pass through the locking hole during surgery, 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 A.L.P.S. mvX Medial Tibia Plate 10H LT (left side) for tibia fractures are affected. Surgeons using this specific model during procedures are at highest risk.
Check for the model number 770715101 on the plate. The product was sold with lot numbers 265814, 24060DF02, 24065DF03, 24060DF01, 24065DF05, or 263512.
Identify the model number (770715101) and lot numbers (265814, 24060DF02, 24065DF03, 24060DF01, 24065DF05, 263512) to confirm if your plate is recalled.
The recall is due to reports of locking screws passing through the locking hole during surgery, causing delays.
The official recall notice does not specify a remedy, so contact Tyber Medical directly for guidance.
Yes, the recalled plates have lot numbers 265814, 24060DF02, 24065DF03, 24060DF01, 24065DF05, or 263512.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1221-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1221-2025 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.
