Tyber Medical recalls A.L.P.S. mvX Medial Tibia Plates due to reports of locking screws passing through holes during surgery, causing delays. Affected units include specific model numbers and lot 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 A.L.P.S. mvX Medial Tibia Plates that may cause locking screws to pass through the locking hole during surgery, leading to delays. This is a serious issue for patients undergoing fracture repair.
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 restarted or adjusted.
Patients who have received the A.L.P.S. mvX Medial Tibia Plate 12H RT for fracture fixation are affected. Surgeons and medical staff using the device during procedures are at higher risk.
Check for model number 770715122, lot numbers 265817, 24060DF08, 263511, 24057DF02, or 24057DF04 on the device. The product is intended for right-side tibia fractures.
Look for model number 770715122 and lot numbers 265817, 24060DF08, 263511, 24057DF02, or 24057DF04 on the device.
The recall is due to complaints that the locking screw passes through the locking hole during surgery, causing delays.
The official notice does not specify a remedy, so contact Tyber Medical directly for guidance.
Yes, model number 770715122 and lot numbers 265817, 24060DF08, 263511, 24057DF02, and 24057DF04 are affected.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1224-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1224-2025 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.
