Tyber Medical recalls A.L.P.S. mvX Anatomic Lateral Fibula Plates (4-hole left) due to reported surgical delays from locking screws passing through holes during use. Affected models include specific lot numbers and catalog 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 certain A.L.P.S. mvX Anatomic Lateral Fibula Plates (4-hole left) because locking screws have been reported to pass through the locking hole during surgery, causing delays. This could lead to longer procedures and potential complications for patients.
During surgery, the locking screw can pass through the locking hole in the plate, causing the device to become unstable. This has led to reported surgical delays as the team must address the issue mid-procedure.
Surgical teams using the recalled plates for fracture fixation are most at risk. Patients undergoing surgery with these specific models may experience longer procedures.
Check for the model number 770708041 on the plate. The affected lot numbers are 24043BU03, 267844, 24043BU02, and 261286. These plates are intended for left-sided fractures of the distal tibia.
Verify the model number on the plate is 770708041.
Reach out to Tyber Medical for guidance on next steps if the plate is affected.
The recall is due to reports that the locking screw passes through the locking hole during surgery, causing delays in procedures.
The affected models are A.L.P.S. mvX Anatomic Lateral Fibula Plates (4-hole left) with model number 770708041 and lot numbers 24043BU03, 267844, 24043BU02, and 261286.
The recall does not require immediate stop use; surgical teams should contact Tyber Medical for guidance if the plate is 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-1209-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1209-2025 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.
