FDA Enforcement
Class II
Ongoing
BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045151
Recall: Z-2063-2023
·
Reported July 12, 2023
Enforcement
- Recall Number
- Z-2063-2023
- Event ID
- 92410
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Report Date
- July 12, 2023
- Initiation Date
- May 4, 2023
- Classification Date
- July 3, 2023
- Address
- Kibbutz Gatton, N/A, GAATON, N/A, N/A, Israel
Description
BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045151
Reason
Drill guides might bend when axial forces are applied by surgeon during procedure and result in potential metal shavings due to friction with the drill bit.Risk to patients includes potential of injury.
Code Info
UDI-DI: 10818674025826 Lot Numbers: 22A01, 22C01,22C02
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Japan, Netherlands.
Quantity
N/A