3-Way Latex Foley Catheter (2017-12-15)

Starting date:

December 15, 2017

Posting date:

January 8, 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-65550

• 
  Reason
• 
  Affected products

Affected Products

3-WAY LATEX FOLEY CATHETER

Reason

To inform customers that a specific product code / lot number combination may potentially have incorrect information printed on the purple retainer cap. The incorrect print specifies that the balloon should be inflated with 10ml of water. However, the correct volume to inflate the balloon catheter is 75cc.

Affected products