Reprocessed Diagnostic Electrophysiology (EP) Catheters (2018-01-25)

Starting date:

January 25, 2018

Posting date:

February 9, 2018

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-65932

• 
  Reason
• 
  Affected products

Affected products

REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER

Reason

Following a product review, Stryker sustainability solutions discovered that it has distributed reprocessed catheters which do not have a Health Canada Medical Device Licence.

Affected products