Reported Feb 14, 2024 · Ongoing

BD BBL Sensi Disc Sulfamethoxazole with Trimethoprim 23.75/1.25 ug, used for semi-quantitative in vitro susceptibility…

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 Sulfamethoxazole with Trimethoprim 23.75/1.25 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231536 and 231539¿
Lot codes and dates
  • Catalog No. 231536 UDI-DI 00382902315360 Lots
    • 1060689
    • 1116935
    • 1210905
    • 1242939
    • 1306103
    • 1334461
    • 2004540
    • 2025116
    • 2056456
    • 2108378
    • 2146453
    • 2301307
    • 3003869
    • 3062089
    • 3094151
    • 3118079
    • 3152968
    • 3248444
    • 0309595
    0343394; Catalog No. 231539¿ UDI-DI 30382902315392 Lots
    • 2339393
    • 3003869
    • 3062089
    • 3094151
    • 3118079
    • 3152968
    • 3214768
    • 3248444
    • 3282335
    • 0309595
    • 0343394
    • 1060689
    • 1116935
    • 1148543
    • 1210905
    • 1242939
    • 1306103
    • 1334461
    • 2004540
    • 2025116
    • 2056456
    • 2108378
    • 2146453
    • 2277321
    • 2301307
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.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Becton Dickinson & Co. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:46 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.