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Beckman Coulter, Inc. recalls MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280
Recalled November 30, 2022 · FDA recall Z-0269-2023 · Beckman Coulter
Hazard
Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect diffuser plate. · FDA Class II
Units
53 plates
Sold at
Worldwide - U.S. Nationwide distribution in the states of AK, FL, IA, ID, MI MS, MT, NC, NE, PA, SC, TX WA, WI, and WV. The countries of Chile, Germany, Indonesia, Italy, Japan, Mexico, Peru, Portugal, South Africa, Spain, United Kingdom of Great Britain and Northern Ireland, and Uruguay.
Description
Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect diffuser plate.
Product
MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280
Manufacturer(s)
Beckman Coulter, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →