---
title: "BD BBL Sensi Disc Moxifloxacin- 5 ug, used for semi-quantitative in vitro sus... — FDA record Z-1035-2024 | Is It on Recall"
description: "There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product dis"
url: https://isitonrecall.com/recall/fda-device-z-1035-2024-bd-bbl-sensi-disc-moxifloxacin-5-ug-used-for-semi-quantitative-in-vitro-susceptibility-testing-catal/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BD BBL Sensi Disc Moxifloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231758¿ — FDA record Z-1035-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 8, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: BD BBL Sensi Disc Moxifloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231758¿
- **Reason**: 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 II
- **Recalling firm**: Becton Dickinson & Co.
- **Quantity**: 2,363,168 total units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1035-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1035-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Catalog No. 231758¿ UDI-DI 30382902317587 Lots 3003061 3243078 1305255 2119637 2153502 2301547 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic distribution nationwide. International distribution worldwide.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Feb 14, 2024
- **Recall initiation date**: Jan 8, 2024
- **Center classification date**: Feb 8, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1035-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Becton Dickinson & Co. records](https://isitonrecall.com/brand/becton-dickinson-co/)
