Z-0758-2016 Class II Terminated

Recalled by Spectranetics Corp. — Colorado Springs, CO

Recall Details

Product Type
Devices
Report Date
February 17, 2016
Initiation Date
January 15, 2016
Termination Date
March 2, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
8 units

Product Description

2.3mm Turbo-Power OTW, Manual, Model No 423-050 Product Usage The Turbo-Power System (Laser Atherectomy Catheter) is a laser atherectomy device designed for use with the CVX-300" Excimer Laser System. The Turbo-Power Laser Atherectomy Catheter is a sterile, single use, prescription only device used for peripheral atherectomy. Turbo-Power is used exclusively with SPNC s CVX 300" Excimer Laser System and is a Type CF device, Defibrillation proof. Turbo-Power is a laser atherectomy catheter designed for treatment of de novo or restenotic lesions in native infrainguinal arteries and for the treatment of femoropopliteal artery in-stent restenosis (ISR) in bare nitinol stents, with adjunctive Percutaneous Transluminal Angioplasty (PTA). Turbo-Power is used to directionally ablate infrainguinal concentric and eccentric lesions in vessels that are 3.5 mm or greater in diameter. The device is comprised of three parts: the working length of the catheter shaft (also the applied part), the motor drive unit (MDU), and the proximal laser shaft which connects the catheter fiber optics to the CVX-300" Excimer Laser System.

Reason for Recall

The product is labeled with an expiration date that is past its shelf life.

Distribution Pattern

Nationwide distribution to Florida, North Carolina and Pennsylvania.

Code Information

Lot CMP15J28A