Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals: Drug Recall

Recall #D-0256-2022 · 09/28/2021

Class III: Low Risk

Recall Details

Recall Number: D-0256-2022
Classification: Class III
Product Type: Drug
Recalling Firm: Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Status: Ongoing
Date Initiated: 09/28/2021
Location: Burbank, CA, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 119 Bottles

Reason for Recall

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

Product Description

Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b) 60-count bottles, NDC: 63629-8392-03, barcode 083923152614; c) 90-count bottles, NDC:63629-8392-04, barcode 083924152614, Lannett Company Inc; Rx only, Packaged by Bryant Ranch Prepack, Burbank, CA 91504.

Distribution Pattern

Nationwide in the USA

Other Recalls by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Class I: Dangerous 10/12/2021

Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Class III: Low Risk 09/28/2021

Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label
Class II: Risk 01/27/2021

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg may contain spironolactone 25 mg tablets.
Class I: Dangerous 01/27/2021

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.

View all recalls by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.