Tyber Medical
83 South Commerce Way, Bethlehem, PA, US
Registered product codes
26 product codes
Recent MDR events
156 on file
- Cannulated Compression Headless ScrewJul 27, 2026Malfunction3012966183-2026-00007
- VOLT¿ WRIST TREATMENT SYSTEMJun 12, 2026Malfunction3012966183-2026-00006
- A.L.P.S. MVX¿May 13, 2026Malfunction3012966183-2026-00005
- CANNULATED SCREW SYSTEM +May 13, 2026Malfunction3012966183-2026-00004
- CANNULATED SCREW SYSTEM +Apr 22, 2026Malfunction3012966183-2026-00003
- TPLIF INTERBODY SYSTEMJan 8, 2026Injury3012966183-2026-00002
- VOLT¿ WRIST TREATMENT SYSTEMJan 7, 2026Malfunction3012966183-2026-00001
- CANNULATED COMPRESSION HEADLESS SCREWOct 10, 2025Injury3012966183-2025-00022
- CANNULATED COMPRESSION HEADLESS SCREWOct 10, 2025Malfunction3012966183-2025-00021
- VOLT¿ WRIST TREATMENT SYSTEMAug 20, 2025Malfunction3012966183-2025-00020
Recalls
20 on file
- Open, ClassifiedJan 20, 2026
The supplier manufactured anatomical left plates with an incorrect thread orientation.
View FDA record ↗ - Open, ClassifiedJan 20, 2026
The supplier manufactured anatomical left plates with an incorrect thread orientation.
View FDA record ↗ - Open, ClassifiedFeb 21, 2025
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
View FDA record ↗ - Open, ClassifiedFeb 21, 2025
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
View FDA record ↗ - Open, ClassifiedFeb 21, 2025
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
View FDA record ↗ - Open, ClassifiedFeb 21, 2025
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
View FDA record ↗ - Open, ClassifiedFeb 21, 2025
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
View FDA record ↗ - Open, ClassifiedFeb 21, 2025
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
View FDA record ↗ - Open, ClassifiedFeb 21, 2025
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
View FDA record ↗ - Open, ClassifiedFeb 21, 2025
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
View FDA record ↗
Compliance history
Matched by FEI 3012966183.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.