Tyber Medical recalls specific medial tibia plates due to reported surgical delays from locking screws passing through holes during use. Affected models include 770715062 with lot numbers 265792, 24053DF01, 24065DF06, 24052DF01.
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 medial tibia plates that may cause surgical delays if the locking screw passes through the locking hole during use. This could lead to longer procedures or complications for patients needing orthopedic surgery.
The locking screw can pass through the locking hole during surgery, causing the plate to become unstable. This has led to reported surgical delays and potential complications for patients.
Patients who have received the specific medial tibia plate model 770715062 with listed lot numbers are most at risk. Surgeons using these plates during procedures may experience delays.
Check for the model number 770715062 on the plate. Look for lot numbers 265792, 24053DF01, 24065DF06, or 24052DF01 on the packaging or device.
Review the model number and lot numbers on the plate to confirm if it is affected.
The recall is due to complaints that the locking screw passes through the locking hole during use, causing surgical delays.
Check the model number and lot numbers to see if it is affected; if so, contact Tyber Medical for guidance.
Yes, the issue can cause surgical delays and potential complications during orthopedic procedures.
We’ve drafted a message you can send Tyber Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1220-2025 — Tyber Medical Tyber Medical Hello, I own a Tyber Medical that is covered by recall Z-1220-2025 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.
