# FDA recall D-0257-2022

> **Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals** · Class III · drug recall initiated 2021-09-28.

## Product

Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC: 71335-1767-09, barcode 083929164865; b) 20-count bottles, NDC: 71335-1767-01, barcode 083921157837; c) 30-count bottles, NDC: 71335-1767-02, barcode 083922165687, d) 60-count bottles, NDC: 71335-1767-03, barcode 083923153776, e) 90-count bottles, NDC: 71335-1767-04, barcode 083924152889, f) 120-count bottles, NDC: 71335-1767-07, barcode 083927153735. Westminster Pharmaceuticals LLC, Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504 USA

## Reason for recall

Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0257-2022
- **Recalling firm:** Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
- **Classification:** Class III
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2021-09-28
- **Report date:** 2021-12-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Burbank, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0257-2022

## Citation

> AI Analytics. FDA recall D-0257-2022. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/D-0257-2022. Source: US FDA. Licensed CC0.

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