PlainRecalls
FDA Devices Moderate Class II Terminated

Reprocessed Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters; Model #: 401450, 401877. Indicated for temporary intracardiac sensing, recording, stimulation, and electrophysiology mapping of cardiac structures.

Reported: June 1, 2016 Initiated: April 28, 2016 #Z-1708-2016

Product Description

Reprocessed Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters; Model #: 401450, 401877. Indicated for temporary intracardiac sensing, recording, stimulation, and electrophysiology mapping of cardiac structures.

Reason for Recall

Mislabeled for size

Details

Units Affected
18 devices
Distribution
Distributed in the state of NY and the country of Canada.
Location
Tempe, AZ

Frequently Asked Questions

What product was recalled?
Reprocessed Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters; Model #: 401450, 401877. Indicated for temporary intracardiac sensing, recording, stimulation, and electrophysiology mapping of cardiac structures.. Recalled by Stryker Sustainability Solutions. Units affected: 18 devices.
Why was this product recalled?
Mislabeled for size
Which agency issued this recall?
This recall was issued by the FDA Devices on June 1, 2016. Severity: Moderate. Recall number: Z-1708-2016.