Health product recall

Neisseria meningitidis Poly A-D (2018-02-28)

Starting date:
February 28, 2018
Posting date:
April 3, 2018
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-66324

Affected products

Neisseria meningitidis Poly A-D

Reason

Remel Neisseria meningitidis Poly A-D (r30166601), lot 2177820 may fail to agglutinate within the specified minimum reaction time when tested with group d Neisseria meningitidis bacteria. However the product continues to correctly identify Neisseria meningitidis groups a, b and c.

Affected products

Neisseria meningitidis Poly A-D

Lot or serial number

2177820

Model or catalog number

R30166601

Companies
Manufacturer
REMEL EUROPE LTD.
Clipper Blvd West Crossways
Dartford, Kent
DA2 6PT
UNITED KINGDOM