Beckman Coulter recalls iPAW 4.2 software version 4.2 (Oct 2015) due to barcode label errors when printing consecutive tube labels. Affected users should check for specific model numbers and contact for updates.
Sorting-Drive software version 4.2 (released in October 2015) introduced a new option for iPAW and the Sorting-Drive Client that is used for manual printing of barcodes. When printing consecutively numbered tube labels using this optional Barcode Counter function, the system incorrectly converts numbers with consecutive multiple zeroes in the middle, potentially leading to wrong barcode IDs. The firm reports that this does not affect automated label creation or reprinting of individual labels and that no other system functions are affected.
Beckman Coulter is recalling software version 4.2 of their iPAW system because it can create incorrect barcode IDs when printing tube labels with consecutive zeros. This error only affects manual label printing and not automated processes.
The software version 4.2 has a bug that misinterprets numbers with consecutive zeros in the middle when printing tube labels. This causes wrong barcode IDs, but does not affect automated label creation or individual label reprinting.
Users of the iPAW 4.2 software who print tube labels manually may be affected. Laboratory technicians handling samples with this software are most at risk.
Check for the iPAW 4.2 User Kit (Part No. B73489) manufactured by Beckman Coulter Biomedical GmbH. The software was released in October 2015 and is used for manual tube label replacement.
Verify your iPAW software version by checking the product documentation or software settings.
No, the issue only affects manual printing of consecutive tube labels with the Barcode Counter function.
The official recall does not mention a fix or remedy; users should check for updates or contact Beckman Coulter.
The affected product is the iPAW 4.2 User Kit with Part No. B73489, manufactured by Beckman Coulter Biomedical GmbH.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-0356-2019 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-0356-2019 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.
