FDA Enforcement Class II Terminated

-Instratek Carpal Tunnel Release Blades, (1) Triangle Blade, (1) Hook Blade. REF R2056 - LOT 122279 -Instratek Carpal Tunnel Release Hook Blade. REF 2055 Lot 122669 -Linvatec CTS Relief Kit. REF 9971, lot 122504 -Biomet Indiana Tome Blade for Carpal Tunnel Release (White). REF 200060. Lot 122504 and Lot 123190. -KMI SafeGuard Knife, For SafeGuard Mini Carpal Tunnel Release System, (White). REF 08-0003. Lot # 122609 Surgical Knife

Recall: Z-1623-2013 · Reported July 10, 2013

Enforcement

Recall Number
Z-1623-2013
Event ID
65205
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Surgical Instrument Service And Savings, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 10, 2013
Initiation Date
May 3, 2013
Classification Date
July 1, 2013
Termination Date
July 11, 2013
Address
2747 Sw 6th St, N/A, Redmond, OR, 97756-7109, United States

Description

-Instratek Carpal Tunnel Release Blades, (1) Triangle Blade, (1) Hook Blade. REF R2056 - LOT 122279 -Instratek Carpal Tunnel Release Hook Blade. REF 2055 Lot 122669 -Linvatec CTS Relief Kit. REF 9971, lot 122504 -Biomet Indiana Tome Blade for Carpal Tunnel Release (White). REF 200060. Lot 122504 and Lot 123190. -KMI SafeGuard Knife, For SafeGuard Mini Carpal Tunnel Release System, (White). REF 08-0003. Lot # 122609 Surgical Knife

Reason

The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.

Code Info

122279; 122493; 122504; 122609; 122669; 123190

Distribution

Nationwide Distribution.

Quantity

56 units