FDA Enforcement Class II Terminated

Reprocessed Daig Steerable and Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters Model Numbers: 401940, 402004 UPC Code: 00885825007409 00885825007744 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit electrical impulses and can be positioned for endocardial recording or stimulation. Diagnostic EP catheters incorporate a handpiece, a flexible shaft and a distal tip section containing diagnostic electrodes. Reprocessed Diagnostic EP Catheters are indicated for temporary intracardiac sensing, recording, stimulation, and electrophysiology mapping of cardiac structures.

Recall: Z-0380-2017 · Reported November 16, 2016

Enforcement

Recall Number
Z-0380-2017
Event ID
75409
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Stryker Sustainability Solutions
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
November 16, 2016
Initiation Date
October 6, 2016
Classification Date
November 9, 2016
Termination Date
December 16, 2016
Address
1810 W Drake Dr, Tempe, AZ, 85283-4327, United States

Description

Reprocessed Daig Steerable and Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters Model Numbers: 401940, 402004 UPC Code: 00885825007409 00885825007744 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit electrical impulses and can be positioned for endocardial recording or stimulation. Diagnostic EP catheters incorporate a handpiece, a flexible shaft and a distal tip section containing diagnostic electrodes. Reprocessed Diagnostic EP Catheters are indicated for temporary intracardiac sensing, recording, stimulation, and electrophysiology mapping of cardiac structures.

Reason

The EP Catheters may be mislabeled for French size during reprocessing.

Code Info

Item Number Serial Number Manufacturing Date 401940 1902898 3/31/2015 401940 1908621 3/31/2015 402004 1902392 1/9/2015 402004 1902389 1/9/2015

Distribution

U.S. distribution to the following; AZ, MN and MO.

Quantity

4 devices