Beckman Coulter Inc. recalls MicroScan WalkAway-96 plus Reconditioned Instrument REF B1018-396R
- Recall date
- October 21, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1088-2022
- 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-96 plus Reconditioned Instrument REF B1018-396R
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