Becton Dickinson recalls BD BBL Sensi Disc Cefaclor for possible inaccuracy in H. influenzae antibiotic testing, risking delayed diagnosis and wrong treatment. Affected lots listed in product description.
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or additional adverse diagnostic outcomes, such as a delay in diagnosis, the selection of inappropriate antibiotics, or extended duration of antibiotic exposure and the treatment process.
Becton Dickinson is recalling BD BBL Sensi Disc Cefaclor discs for possible inaccuracy in testing for H. influenzae. This could lead to delayed diagnosis, wrong antibiotic choices, or longer treatment times. The recall affects specific lots sold in 2004-2005.
The discs may cause inaccurate results for H. influenzae testing, leading to potential delays in diagnosis or incorrect antibiotic selection. This could result in longer treatment times or inappropriate antibiotic use.
Healthcare professionals using the discs for antibiotic susceptibility testing are most at risk. The recall affects specific lots sold between 2004 and 2005.
Check the product label for catalog number 231653¿ or lot numbers 1085898, 1273095, 1273096, 2004485, 2147706, 2333108. The discs were sold between 2004 and 2005.
Look for catalog number 231653¿ or specific lot numbers listed in the recall notice.
The discs may cause inaccurate results for H. influenzae testing, potentially leading to delayed diagnosis or wrong antibiotic choices.
Check the product label for the catalog number or lot numbers listed in the recall notice. If affected, contact Becton Dickinson for guidance.
The recall addresses potential testing inaccuracies, not physical safety risks. There is no immediate danger to users.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-1017-2024 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-1017-2024 from Becton Dickinson. 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.
