Tyber Medical 2025-03-05 Health serious FDA
Health · FDA · Recall #FDA-Z-1222-2025
A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right Intended… Recall
Issued March 5, 2025 · Tyber Medical
In March 2025, Tyber Medical recalled the A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right Intended…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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
What you should do
- 1 Stop using A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right Intended… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Tyber Medical to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Tyber Medical
- Category
- Health
- Recall date
- March 5, 2025
- Units affected
- Not reported
- Sold at
- Nationwide
- Recall number
- FDA-Z-1222-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Tyber Medical has 5 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.