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 770715121 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 A.L.P.S. mvX Medial Tibia plates that may cause surgical delays if the locking screw passes through the intended hole during use. This could lead to complications during fracture repair procedures.
The locking screw can pass through the intended locking hole during surgery, causing delays in the procedure. This may lead to complications in fixing fractures of the distal tibia.
Orthopedic surgeons and medical professionals who use these plates for fracture fixation are most at risk. Patients receiving this specific implant during surgery may be affected.
Check for model number 770715121 with lot numbers 265816, 24064DF01, 263557, 24065DF04, 24059DF03, or 24059DF02. These plates are intended for left tibia fractures.
Verify the model number and lot numbers listed in the recall notice to confirm if your device is affected.
The recall is due to complaints that the locking screw passes through the locking hole during use, causing surgical delays in fixing tibia fractures.
The official recall notice does not specify a remedy or action steps for affected devices.
Yes, affected lot numbers include 265816, 24064DF01, 263557, 24065DF04, 24059DF03, and 24059DF02.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1223-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1223-2025 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.
