Coagulation Factor V Deficient Plasma (2020-04-04)

Starting date:

April 4, 2020

Posting date:

April 24, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-72869

Last updated: 2020-04-24

• Reason
• Affected products

Affected Products

Coagulation Factor V Deficient Plasma

Reason

Device packages may contain incorrect vials, which lead to control results out of range.

Affected products