Reported Feb 14, 2024 · Ongoing

BD BBL Sensi Disc Tetracycline 30 ug,used for semi-quantitative in vitro susceptibility testing. Catalog Number 230998…

Becton Dickinson & Co.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Becton Dickinson & Co. · 7 Loveton Cir · Sparks, MD · 21152-9212

Is this the product you have?

  • BD BBL Sensi Disc Tetracycline 30 ug,used for semi-quantitative in vitro susceptibility testing. Catalog Number 230998 and 231344¿
Lot codes and dates
  • Catalog No. 230998 UDI-DI 00382902309987 Lots
    • 1242880
    • 1277918
    • 1301570
    • 2025088
    • 2056233
    • 2118569
    • 2276681
    • 3094187
    • 3212760
    • 3263267
    • 9009914
    • 9046895
    • 0065366
    0178210; Catalog No. 231344¿ UDI-DI 30382902313442 Lots
    • 3010027
    • 3062263
    • 3094187
    • 3158029
    • 3212760
    • 3263267
    • 3275644
    • 0065366
    • 0085202
    • 0230453
    • 0274792
    • 0335906
    • 1095603
    • 1148539
    • 1180271
    • 1242880
    • 1277918
    • 1301570
    • 2025088
    • 2056233
    • 2089874
    • 2118569
    • 2276681
    • 8355562
    • 9009914
    • 9046895
    • 9130797
    • 9239639
    • 9263061
Amount recalled
2,363,168 total units

This recall covers 30 products

The agency filed one notice per product. You are reading one of them; the other 29 are below.

17 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:19 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.