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