Beckman Coulter recalls MicroScan WalkAway-96 Plus instruments with incorrect 1-ampere power connector that may cause overheating. Affected units have specific serial numbers and catalog codes.
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
Beckman Coulter is recalling MicroScan WalkAway-96 Plus instruments that may have an incorrect power connector rated at 1 ampere instead of the required 10 ampere. This could lead to overheating and potential damage if the instrument is used improperly.
The instrument may have been assembled with a power connector rated at 1 ampere instead of the correct 10 ampere rating. This could cause overheating if the instrument is used with a higher current load than the connector can handle.
Lab technicians and healthcare professionals using the MicroScan WalkAway-96 Plus instrument are most at risk. Affected units have specific serial numbers and catalog codes.
Check for serial numbers 39610007 through 39610013 or catalog code B1018-284. The UDI-DI code is 15099590658687.
Look for serial numbers 39610007 through 39610013 on the instrument.
Reach out to Beckman Coulter for further assistance if you have the affected serial numbers.
The MicroScan WalkAway-96 Plus Instrument with reference number B1018-284.
Check for serial numbers 39610007 through 39610013 or catalog code B1018-284.
Contact Beckman Coulter for further assistance if you have the affected serial numbers.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1084-2022 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1084-2022 from Beckman Coulter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
