IH-QC (2019-09-13)

Starting date:

September 13, 2019

Posting date:

November 15, 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-71589

Last updated: 2019-11-15

• Reason
• Affected products

Affected Products

IH-QC

Reason

Weak reactions and sometimes negative results were observed when the antibody was used against enzymatic-treated positive D cells (papain) only with the NaCl, enzyme test and cold agglutinins ID-cards. Catalog 005014, m 006026, 005016 and 005017).

Affected products