# FDA recall D-1059-2016

> **Valeant Pharmaceuticals North America LLC** · Class III · drug recall initiated 2016-06-10.

## Product

SECONAL SODIUM (secobarbital sodium) Capsules, USP, 100 mg, 100 Ct. Bottles, Rx Only. Distributed by: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ 08807. NDC: 0187-4220-10.

## Reason for recall

Labeling: Incorrect or Missing Package Insert: Package insert is missing warning regarding anaphylaxis.

## Distribution

US Nationwide

## Key facts

- **Recall number:** D-1059-2016
- **Recalling firm:** Valeant Pharmaceuticals North America LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-06-10
- **Report date:** 2016-07-06
- **Termination date:** 2017-06-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bridgewater, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1059-2016

## Citation

> AI Analytics. FDA recall D-1059-2016. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1059-2016. Source: US FDA. Licensed CC0.

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