Tyber Medical recalls ANATOMIC LAT FIB PLATE 10H LT for reported surgical delays due to locking screw issues during use. Affected models include 770708101 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 specific type of orthopedic plate used in surgeries for potential surgical delays caused by locking screws passing through the locking hole. This could lead to longer procedures or complications if the device is used without addressing the issue.
The locking screw may pass through the locking hole during surgery, causing delays. This issue has been reported in clinical use, potentially leading to extended procedures or complications.
Orthopedic surgeons and medical facilities using the ANATOMIC LAT FIB PLATE 10H LT model for left-sided fractures. Those with the specific lot numbers listed are most at risk.
Check for the model number 770708101 on the device. Look for lot numbers 269171, 265809, 262558, or 260891. The product is intended for fixing fractures of the distal tibia.
Verify the model number is 770708101 and the lot number matches one of the listed numbers: 269171, 265809, 262558, or 260891.
The recall is due to complaints that the locking screw passes through the locking hole during surgery, causing reported delays in procedures.
The official recall notice does not specify a remedy or action steps for affected devices.
Lot numbers 269171, 265809, 262558, and 260891 are 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-1215-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1215-2025 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.
