# FDA recall D-1042-2018

> **Morton Grove Pharmaceuticals, Inc.** · Class II · drug recall initiated 2018-07-24.

## Product

Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, 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

Defective Container:  Tamper Evident  foil seal not completely intact.

## Distribution

U.S. Nationwide

## Key facts

- **Recall number:** D-1042-2018
- **Recalling firm:** Morton Grove Pharmaceuticals, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-07-24
- **Report date:** 2018-08-15
- **Termination date:** 2022-09-09

- **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-1042-2018

## Citation

> AI Analytics. FDA recall D-1042-2018. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-1042-2018. Source: US FDA. Licensed CC0.

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