Beckman Coulter recalls DxM 1096 MicroScan WalkAway Instruments with incorrect 1-amp power connector that may cause overheating. Affected units have specific serial numbers.
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 DxM 1096 MicroScan WalkAway Instruments that may have been assembled with a power connector rated at 1 ampere instead of the required 10 ampere. This could lead to overheating and potential fire hazards if the instrument is used normally.
The instrument may have a power connector rated at 1 ampere instead of the correct 10 ampere rating. This incorrect connector could overheat when the instrument is used, potentially causing a fire hazard.
Users of the DxM 1096 MicroScan WalkAway Instrument with specific serial numbers listed in the recall. Laboratory technicians and healthcare professionals using this equipment are most at risk.
Check for the serial numbers listed in the recall: 49610039 through 49610091 (excluding 49610061). The product is a DxM 1096 MicroScan WalkAway Instrument with reference number B1018-496.
Verify your instrument's serial number against the list of affected units provided in the recall notice.
The power connector may be rated at 1 ampere instead of the required 10 ampere, which could cause overheating and fire hazards.
Check if your serial number is in the list: 49610039 through 49610091 (excluding 49610061).
The recall does not specify a remedy, so contact Beckman Coulter directly for guidance.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1086-2022 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1086-2022 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.
