Medical device recalls Moderate risk

Abbott Laboratories, Inc recalls Abbott ARCHITECT Creatine Kinase, IVD, REF 7D6341.

Recall date
July 18, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1076-2019
FDA classification
Class II
Brand / firm
Abbott Laboratories, Inc
Sold / distributed
Distribution was made nationwide, including Puerto Rico. There was also government and military distribution. Foreign distribution was made to Algeria, Argentina, Australia, Austria, Belarus, Belgium, Bermuda, Bosnia and Herzegovina, Brazil, Brunei, Bulgaria, Canada, Cayman Islands, Chile, China, C…

Why it was recalled

The product has a stability issue which may lead to an error code indicating "Unable to calculate result, reaction check failure" and/or Quality Control results out of range low.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Abbott ARCHITECT Creatine Kinase, IVD, REF 7D6341.

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