Tyber Medical recalls specific 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 specific model of Anatomic Lateral Fibula Plate for surgical use. The recall is due to complaints that the locking screw can pass through the locking hole during surgery, causing delays.
The locking screw may pass through the locking hole during surgery, leading to the need for additional procedures. This has resulted in reported surgical delays for patients using the recalled device.
Surgical teams using the specific model of Anatomic Lateral Fibula Plate for orthopedic procedures are affected. Patients undergoing surgery with this device are at risk of delayed procedures.
Check for the model name 'Anatomic Lateral Fibula Plate, 4-hole, Right' with catalog number 770708042. Lot numbers 267845, 261287, 265780, and 24033BU01 are also associated with this recall.
Verify the model name, catalog 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 can pass through the locking hole during surgery, causing reported surgical delays.
The official recall notice does not specify a remedy or action for affected devices.
The recall mentions surgical delays but does not describe a risk of serious injury or harm to patients.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1210-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1210-2025 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.
