BD Biosciences recalls BD Multitest 6-Color TBNK with optional Trucount Tubes (Cat. No. 662995) due to partial label detachment that can cause tubes to stick together or automation errors in flow cytometers.
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.
BD Biosciences is recalling BD Multitest 6-Color TBNK with optional Trucount Tubes (Cat. No. 662995) because partial label detachment may cause tubes to become stuck together or lead to automation errors when used with flow cytometers. This could affect lab results and require corrective action.
Partial label detachment on the tubes can cause them to stick together in the pouch. This may lead to automation errors when the tubes are used with the automated loader for the wash assistant in flow cytometers, potentially affecting lab results.
Lab users who own or use BD Multitest 6-Color TBNK with optional Trucount Tubes (Cat. No. 662995) for flow cytometry. Researchers and lab technicians handling blood samples are most at risk.
Check for BD Multitest 6-Color TBNK with optional Trucount Tubes (Cat. No. 662995) sold for BD FACSLyric, BD FACSCanto II, and BD FACSCanto flow cytometers. Lot numbers 11568, 45905, 53637, 88003, 89111, and 31905 are affected.
Verify the product name and lot numbers to confirm if your item is affected.
Partial label detachment can cause tubes to become stuck together in the pouch or lead to automation errors when used with the automated loader for the wash assistant.
BD FACSLyric, BD FACSCanto II, and BD FACSCanto flow cytometers.
The recall does not specify a remedy, so contact BD Biosciences for guidance.
We’ve drafted a message you can send BD Biosciences to request your refund or repair — edit it as you like.
Subject: Recall Z-0173-2023 — BD Biosciences BD Biosciences Hello, I own a BD Biosciences that is covered by recall Z-0173-2023 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.
