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