EZ PRO Swab Kit (2020-04-11)

Starting date:

April 11, 2020

Posting date:

April 21, 2020

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-72875

Last updated: 2020-07-10

• Reason
• Affected products

Affected Products

EZ PRO Swab Kit

Reason

Media tubes and swabs may not have been adequately sterilized in accordance with published sterilization standards and may be contaminated.

Affected products