# FDA recall D-0130-2020

> **Morton Grove Pharmaceuticals, Inc.** · Class II · drug recall initiated 2019-09-23.

## Product

Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, packaged in a 8 fl oz (237 mL) bottle, Rx only, Manufactured By Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053. NDC 60432-212-08

## Reason for recall

Failed Impurities/Degradation Specifications - failed specs for Prednisolone Impurity 14

## Distribution

Nationwide USA and Puerto Rico

## Key facts

- **Recall number:** D-0130-2020
- **Recalling firm:** Morton Grove Pharmaceuticals, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-09-23
- **Report date:** 2019-10-16
- **Termination date:** 2022-09-24

- **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-0130-2020

## Citation

> AI Analytics. FDA recall D-0130-2020. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/D-0130-2020. Source: US FDA. Licensed CC0.

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