Health product recall

Rheumatoid Factor (RF) Latex test (2018-02-20)

Starting date:
February 20, 2018
Posting date:
March 13, 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-66150

Affected products

RHEUMATOID FACTOR (RF) LATEX TEST

Reason

The RF latex in these kits may yield a weak positive result on negative specimens.

Affected products

RHEUMATOID FACTOR (RF) LATEX TEST

Lot or serial number

656
656001
656002

Model or catalog number

10502
10502PK
10503
10512

Companies
Manufacturer
Pulse Scientific Inc.
5100 South Service RD, Unit 18
Burlington
L7L 6A5
CANADA