Beckman Coulter recalls 100+ UniCel DxI 800 photometric analyzers with specific part numbers and serials due to potential z-axis movement errors causing delays in test results.
An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not Ready or Paused state, leading to a delay in obtaining results.
Beckman Coulter is recalling 100+ UniCel DxI 800 photometric analyzers that may enter a 'Not Ready' or 'Paused' state due to defective internal components, causing delays in test results. This does not pose a safety risk but could affect lab testing timelines.
Defective sub-components in the gantry assembly can cause the analyzer to temporarily stop working, delaying test results without causing injury or damage to the user.
Lab users with the specific part numbers and serials listed in the recall notice. The risk is minimal as it only affects test timing, not safety.
Check for part numbers 973100 or A71456, or serial numbers listed in the recall notice. The device is sold as a photometric chemistry analyzer for laboratory use.
Verify your device's part numbers (973100, A71456) or serial numbers against the list provided in the recall notice.
No, this recall does not pose a safety risk. The issue only causes delays in test results, not injuries or damage.
Check your device's part numbers (973100 or A71456) or serial numbers against the list provided in the recall notice.
No action is required for this recall. The issue only affects test timing, not safety.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-0429-2026 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-0429-2026 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.
