Tyber Medical recalls A.L.P.S. mvX Medial Tibia Plates with 16 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 with 16 holes for left tibia fractures. The recall is due to complaints that the locking screw can pass through the locking hole during surgery, causing delays.
The locking screw can pass through the locking hole during surgery, which has led to reported surgical delays. This issue occurs with the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula devices.
Orthopedic surgeons and medical professionals who use these plates for tibia fracture fixation are most at risk. Patients receiving this specific surgical implant may also be affected.
Check for the model number 770715161 on the plate. The lot numbers 24061DF01, 24065DF02, and 24070DF01 are also associated with this recall.
Reach out to Tyber Medical directly for guidance on the recall and potential remedies.
The recall is due to complaints that the locking screw can pass through the locking hole during surgery, causing reported surgical delays.
The affected model number is 770715161 with lot numbers 24061DF01, 24065DF02, and 24070DF01.
Check the model number on the plate, which should be 770715161, and verify the lot numbers 24061DF01, 24065DF02, or 24070DF01.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1225-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1225-2025 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.
