FDA Enforcement
Class II
Terminated
ORTHOCORD One Violet and One Blue Braided Composite Suture with MO-7 Taper Needles, Catalog Number: 223114. For use in general soft tissue approximation, and/or ligation, including orthopedic procedures.
Recall: Z-1174-2013
·
Reported May 1, 2013
Enforcement
- Recall Number
- Z-1174-2013
- Event ID
- 64706
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- DePuy Mitek, Inc., a Johnson & Johnson Co.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- May 1, 2013
- Initiation Date
- March 22, 2013
- Classification Date
- April 25, 2013
- Termination Date
- February 24, 2014
- Address
- 325 Paramount Drive, Raynham, MA, 02767-5199, United States
Description
ORTHOCORD One Violet and One Blue Braided Composite Suture with MO-7 Taper Needles, Catalog Number: 223114. For use in general soft tissue approximation, and/or ligation, including orthopedic procedures.
Reason
The IFU provided with the free strand ORTHOCORD sutures currently indicates that approximately 100% suture strength remains at six weeks after implantation. While this statement is true for Violet ORTHOCORD sutures, it is an inaccurate statement for Blue ORTHOCORD free strand sutures. Based on in-vivo strength retention study, a Blue ORTHOCORD sutures maintain approximately 80% of strength at six
Code Info
ALL from Jan 1 2010 - Corrected IFU implementation date
Distribution
Nationwide Distribution.
Quantity
206540