FDA Enforcement
Class II
Terminated
SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Product Code: 72203842 Fastener, fixation, nondegradable, soft tissue
Recall: Z-2046-2014
·
Reported July 23, 2014
Enforcement
- Recall Number
- Z-2046-2014
- Event ID
- 68565
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Smith & Nephew, Inc. Endoscopy Division
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- July 23, 2014
- Initiation Date
- June 2, 2014
- Classification Date
- July 14, 2014
- Termination Date
- September 15, 2017
- Address
- 150 Minuteman Drive, N/A, Andover, MA, 01810-1031, United States
Description
SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Product Code: 72203842 Fastener, fixation, nondegradable, soft tissue
Reason
Sterility of device is compromised due to breach in sterile barrier
Code Info
Lot Numbers: 50477397, 50481448
Distribution
Worldwide Distribution - USA (nationwide) and Internationally to Australia, Belgium, Denmark, France, Germany, Great Britain, Italy, Netherlands, Norway, Portugal, Spain, and Sweden.
Quantity
136 units