# FDA recall D-1283-2015

> **Teva Pharmaceuticals USA** · Class II · drug recall initiated 2015-06-24.

## Product

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, (CII), 10 mg   (Mixed Salts of a Single Entity Amphetamine Product), 100 count bottles, manufactured at Barr Laboratories, Inc. Forest, VA for Teva Pharmaceuticals USA, Sellersville, PA --- NDC 0555-0972-02

## Reason for recall

Failed Impurities/Degradation Specifications: out of specification for unknown impurity

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1283-2015
- **Recalling firm:** Teva Pharmaceuticals USA
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-06-24
- **Report date:** 2015-08-12
- **Termination date:** 2016-08-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Horsham, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1283-2015

## Citation

> AI Analytics. FDA recall D-1283-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1283-2015. Source: US FDA. Licensed CC0.

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