Beckman Coulter recalls DxM 1040 MicroScan WalkAway Instruments with incorrect 1-amp power connector that may cause electrical issues. Affected units have specific serial numbers and model 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 certain DxM 1040 MicroScan WalkAway Instruments due to a potential electrical hazard from an incorrectly installed power connector. This could lead to improper power handling and possible electrical issues if the instrument is used.
The instrument may have been assembled with a power connector rated for only 1 ampere instead of the required 10 ampere current rating. This mismatch could cause improper power handling, potentially leading to electrical issues or malfunctions.
Users of the DxM 1040 MicroScan WalkAway Instrument with specific serial numbers and model codes are affected. Laboratory technicians and medical professionals using these instruments are most at risk.
Check for the model number DxM 1040 MicroScan WalkAway Instrument with serial numbers starting with 44010026 through 44010068. The specific UDI-DI code 15099590690885 also identifies affected units.
Look for serial numbers starting with 44010026 through 44010068 on the instrument.
Confirm the model code is DxM 1040 MicroScan WalkAway Instrument with UDI-DI code 15099590690885.
The recalled model is the DxM 1040 MicroScan WalkAway Instrument with serial numbers starting with 44010026 through 44010068.
The instrument may have an incorrectly installed power connector rated at 1 ampere instead of the required 10 ampere current rating, which could cause electrical issues.
Check for serial numbers starting with 44010026 through 44010068 and the UDI-DI code 15099590690885.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1085-2022 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1085-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
