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Serious recall: Injury is possible or has been reported. Take action promptly.

Becton Dickinson & Co. 2024-02-14 Health serious FDA
Health · FDA · Recall #FDA-Z-1037-2024

BD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug, used for semi-quantitative in… Recall

Issued February 14, 2024 · Becton Dickinson & Co.

In February 2024, Becton Dickinson & Co. recalled the BD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug, used for semi-quantitative in…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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.

What you should do

  1. 1 Stop using BD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug, used for semi-quantitative in… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Becton Dickinson & Co. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Becton Dickinson & Co.
Category
Health
Recall date
February 14, 2024
Units affected
Not reported
Sold at
Domestic distribution nationwide. International distribution worldwide.
Recall number
FDA-Z-1037-2024
Made in
United States
Issuing agency
FDA

In context

  • Becton Dickinson & Co. has 7 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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