# FDA recall D-0696-2017

> **Akorn Inc** · Class II · drug recall initiated 2017-03-13.

## Product

Sulfamethoxazole and Trimethoprim Oral Suspension, USP 200 mg / 40 mg per 5 mL , Grape Flavor, Rx Only, 16 fl oz. (473 mL), HI-TECH PHARMACAL CO., INIC, Amityville, NY 11701, NDC 50383-824-16

## Reason for recall

Failed Dissolution Specifications

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0696-2017
- **Recalling firm:** Akorn Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-03-13
- **Report date:** 2017-05-10
- **Termination date:** 2019-07-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lake Forest, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0696-2017

## Citation

> AI Analytics. FDA recall D-0696-2017. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0696-2017. Source: US FDA. Licensed CC0.

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