BD BBL Sensi Disc Levofloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231705 and 231706¿

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Catalog No. 231705 UDI-DI 00382902317050 Lots 1334510 2004644 2091272 2277179 3030830 3094117 3248344; Catalog No. 231706¿ UDI-DI 30382902317068 Lots 2277179 3030830 3094117 3184118 3248344 1334510 2004644 2091272 2213599
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Becton Dickinson & Co.
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

BD BBL Sensi Disc Levofloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231705 and 231706¿

Product Codes/Lot Numbers:

Catalog No. 231705 UDI-DI 00382902317050 Lots 1334510 2004644 2091272 2277179 3030830 3094117 3248344; Catalog No. 231706¿ UDI-DI 30382902317068 Lots 2277179 3030830 3094117 3184118 3248344 1334510 2004644 2091272 2213599

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1032-2024

Related Recalls

Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.

Sep 23, 2025 Other Medical Devices Nationwide View Details →

Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.

Sep 23, 2025 Surgical Instruments Nationwide View Details →