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Health product recall

Vitros Performance Verifier II

Starting date:
July 13, 2017
Posting date:
August 14, 2017
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-64162

Reason

Ortho Clinical Diagnostics has determined that the unopened storage condition for Vitros Performance Verifier II, Lot K4852 (only) requires revision when using Vitros Chemistry products AST slides.

Affected products

Vitros Performance Verifier II

Lot or serial number

K4852

Model or catalog number

8231474

Companies

Manufacturer
Ortho-Clinical Diagnostics Inc.
100 Indigo Creek Drive
Rochester
14626
New York
UNITED STATES