Drug recall
Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC: 71335-1767-09, barcode…
FDA recall event 88847 · Class III · Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Key facts
| Event ID | 88847 |
|---|---|
| Recall numbers | D-0256-2022, D-0257-2022 |
| Recalling firm | Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals |
| Product type | Drugs |
| Products | 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…, 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… |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label |
| Initiation date | Sep 28, 2021 |
| Report date | Dec 1, 2021 |
| City | Burbank |
| State | CA |
| Country | United States |
| FEI number | 1000519407 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: