BD Biosciences recalls BD Trucount Tubes (Cat. No. 663028) due to partial label detachment that may cause tubes to stick together or automation errors in blood cell counting.
Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation errors when used with the automated loader for the wash assistant. Firm root cause investigation confirmed that label detachment is due to an adhesive change by a tier 2 supplier.
BD Biosciences is recalling BD Trucount Tubes (Cat. No. 663028) used for blood leukocyte counting because the label can detach, potentially causing tubes to stick together or causing errors in automated blood testing equipment.
Partial label detachment can cause tubes to become stuck together in the pouch or lead to automation errors when used with the BD FACS Loader. This is due to an adhesive change by a tier 2 supplier.
Users of BD Trucount Tubes for blood cell counting in labs or medical settings. Those using the tubes with automated systems are most at risk of errors.
Check for BD Trucount Tubes with catalog number 663028. Lot numbers 2031238, 2063994, 2095615, 2145791, 2221697, and 2237045 are affected.
Verify the catalog number and lot numbers to confirm if your tubes are affected.
The label can partially detach, causing tubes to stick together or automation errors in blood cell counting systems.
Tubes may become stuck together in the pouch or cause errors when used with the automated loader for blood testing.
Check for catalog number 663028 and lot numbers 2031238, 2063994, 2095615, 2145791, 2221697, or 2237045.
We’ve drafted a message you can send BD Biosciences to request your refund or repair — edit it as you like.
Subject: Recall Z-0172-2023 — BD Biosciences BD Biosciences Hello, I own a BD Biosciences that is covered by recall Z-0172-2023 from BD Biosciences. 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.
