ADT1018 FlowQC Tubing (TRANSONIC SYSTEMS FLOWMETER) (2019-02-12)

Starting date:

February 12, 2019

Posting date:

May 3, 2019

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-69800

Last updated: 2019-05-03

• Reason
• Affected products

Affected Products

ADT1018 FlowQC Tubing (TRANSONIC SYSTEMS FLOWMETER)

Reason

Transonic became aware that ADT1018 was likely to have been uncontrolled at the manufacturing facility. Upon receiving this information, Transonic conducted a Health Risk Analysis and found that the removal of ADT1018 was necessary due to the potential risk involved.

Affected products