Pro-Vent Plus Arterial Blood Sampling Kit (2020-01-07)

Starting date:

January 7, 2020

Posting date:

January 24, 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-72181

Last updated: 2020-01-24

• Reason
• Affected products

Affected Products

Pro-Vent Plus Arterial Blood Sampling Kit

Reason

Specific lots of Portex Pro-Vent and Linedraw Arterial Blood Sampling Syringes may have broken luers.

Affected products