Beckman Coulter recalls reconditioned MicroScan WalkAway-40 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 reconditioned MicroScan WalkAway-40 plus instruments that may have an incorrect power connector rated at 1 ampere instead of the required 10 ampere. This could cause overheating and potential damage if used normally.
The instrument may have been assembled with a power connector rated at 1 ampere instead of the correct 10 ampere rating. This incorrect connector could overheat during normal use, potentially causing damage to the instrument or electrical hazards.
Users of reconditioned MicroScan WalkAway-40 plus instruments with specific serial numbers and catalog codes are affected. Laboratory technicians and medical professionals using these instruments are most at risk.
Check for the catalog number B1018-340R and serial numbers 34020035, 34020224, or 34030054. The UDI-DI code 15099590684112 is also associated with these units.
Verify your MicroScan WalkAway-40 plus has the catalog number B1018-340R and one of the serial numbers listed.
The power connector may be rated at 1 ampere instead of the required 10 ampere, which could cause overheating.
Check for the catalog number B1018-340R and serial numbers 34020035, 34020224, or 34030054.
The recall record does not specify a remedy, so contact Beckman Coulter for further instructions.
We’ve drafted a message you can send Beckman Coul: a short, human brand name for headings (e.g. to request your refund or repair — edit it as you like.
Subject: Recall Z-1087-2022 — Beckman Coul: a short, human brand name for headings (e.g. Beckman Coul: a short, human brand name Hello, I own a Beckman Coul: a short, human brand name for headings (e.g. that is covered by recall Z-1087-2022 from Beckman Coul: a short, human brand name for headings (e.g.. 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.
