# FDA recall D-0713-2022

> **Morton Grove Pharmaceuticals, Inc.** · Class II · drug recall initiated 2022-02-21.

## Product

Dexamethasone Elixir, USP 0.5 mg/5 mL, Net: 8 fl oz (237 mL) bottle, Rx only, Manufactured By: Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053, NDC 60432-466-08.

## Reason for recall

Failed Impurities/Degradation Specifications: higher than permissible levels of unknown impurities were found in the drug product.

## Distribution

Nationwide USA and Puerto Rico

## Key facts

- **Recall number:** D-0713-2022
- **Recalling firm:** Morton Grove Pharmaceuticals, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-02-21
- **Report date:** 2022-03-09
- **Termination date:** 2024-08-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morton Grove, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0713-2022

## Citation

> AI Analytics. FDA recall D-0713-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0713-2022. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
