Stryker Sustainability Solutions: Medical Device Recall in 2016 - (Recall #: Z-1708-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: April 28, 2016

Date Posted: June 1, 2016

Recall Number: Z-1708-2016

Event ID: 73983

Reason for Recall:

Mislabeled for size

Status: Terminated

Product Quantity: 18 devices

Code Information:

Catalog Number: 401450 Lot Number: 2561683E Expiration Date: 5/13/2017 Catalog Number: 401877 Lot Number: 2555866E Expiration Date: 5/6/2017

Distribution Pattern:

Distributed in the state of NY and the country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated