Tyber Medical recalls A.L.P.S. mvX Anatomic Lateral Fibula Plates 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 Anatomic Lateral Fibula Plates because locking screws can pass through the locking hole during surgery, causing delays. This risk affects patients undergoing fracture fixation procedures.
During surgery, the locking screw can pass through the locking hole in the plate, which may cause surgical delays. This issue has been reported in clinical use but does not typically cause serious injury.
Patients who have received the A.L.P.S. mvX Anatomic Lateral Fibula Plate for fracture fixation are most at risk. Healthcare providers using these plates in surgeries may also be affected.
Check for the model number 770708061 on the plate. The product was sold with lot numbers 267846, 265782, 24043BU04, and 261288.
Identify the model number (770708061) and lot numbers (267846, 265782, 24043BU04, 261288) to confirm if your plate is affected.
The recall reports surgical delays but does not indicate serious injury. The hazard is not severe enough to require immediate stop use.
Check for model number 770708061 and lot numbers 267846, 265782, 24043BU04, or 261288.
No immediate stop is required. The recall asks for identification but does not specify discarding or returning the product.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1211-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1211-2025 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.
