Medical device recalls Moderate risk

Beckman Coulter Inc. recalls MicroScan WalkAway-40 plus Reconditioned Instrument REF B1018-340R

Recall date
October 21, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1087-2022
FDA classification
Class II
Brand / firm
Beckman Coulter Inc.
Sold / distributed
Worldwide distribution - U.S. Nationwide distribution in the states of Alaska, Arkansas, California, Colorado, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maine, Maryland, Michigan, Minnesota, Missouri, New Jersey, New Mexico, New York, North Carolin…

Why it was recalled

WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10 ampere

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

What was recalled

MicroScan WalkAway-40 plus Reconditioned Instrument REF B1018-340R

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