PlainRecalls
FDA Devices Moderate Class II Ongoing

MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280

Reported: November 30, 2022 Initiated: October 3, 2022 #Z-0269-2023

Product Description

MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280

Reason for Recall

Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect diffuser plate.

Details

Recalling Firm
Beckman Coulter, Inc.
Units Affected
53 plates
Distribution
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.
Location
West Sacramento, CA

Frequently Asked Questions

What product was recalled?
MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280. Recalled by Beckman Coulter, Inc.. Units affected: 53 plates.
Why was this product recalled?
Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect diffuser plate.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 30, 2022. Severity: Moderate. Recall number: Z-0269-2023.