FDA Enforcement
Class II
Terminated
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 3 Hole Plate Item Number: 2110-135-003 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures
Recall: Z-3262-2018
·
Reported October 3, 2018
Enforcement
- Recall Number
- Z-3262-2018
- Event ID
- 80921
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Biomet UK Ltd.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Report Date
- October 3, 2018
- Initiation Date
- August 9, 2018
- Classification Date
- September 27, 2018
- Termination Date
- May 12, 2020
- Address
- Waterton Industrial Estate, Bridgend, N/A, United Kingdom
Description
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 3 Hole Plate Item Number: 2110-135-003 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures
Reason
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
Code Info
Lot Number: 3680822 3680823 3680824 3680825 3700273
Distribution
US Nationwide in the states of AZ, MO, NJ and NM
Quantity
10 units