Butalbital — Class III drug recall D-0257-2022
Ongoing recall by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals, reported 2021-12-01, distributed nationwide. Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label
| Recall number | D-0257-2022 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals, Burbank, CA, United States |
| Recall initiated | 2021-09-28 |
| Classified | 2021-11-23 |
| Reported by FDA | 2021-12-01 |
| Distributed | Nationwide (US) |
| Quantity | 574 bottles |
| Reason classes | labeling |
| NDC | 71335-1767-01, 71335-1767-02, 71335-1767-03, 71335-1767-04, 71335-1767-07, 71335-1767-09 |
| Lot numbers | 151160, 151338, 152156, 152197, 152245, 152347, 152889, 153735, 153776, 154380, 154997, 155752, 157837, 158841, 159345, 159352, 159943, 159973, 160004, 160330, 160419, 162113, 162641, 164865, 165687 |
| Expiration dates | 2021-02-28, 2022-07-31, 2022-08-31, 2023-02-28 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0257-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.