Liberator (2020-05-01)

Starting date:

May 1, 2020

Posting date:

June 12, 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-73295

Last updated: 2020-06-12

• Reason
• Affected products

Affected Products

Liberator

Reason

An evaluation of the manufacturing process has identified a potential failure that could present a safety concern. There have been no injuries or reported defects associated with this potential issue.

Affected products