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.
Reported: August 15, 2018 Initiated: July 24, 2018 #D-1042-2018
Product Description
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.
Details
- Recalling Firm
- Morton Grove Pharmaceuticals, Inc.
- Units Affected
- 38,280 bottles
- Distribution
- U.S. Nationwide
- Location
- Morton Grove, IL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Morton Grove Pharmaceuticals, Inc.. Units affected: 38,280 bottles.
Why was this product recalled? ▼
Defective Container: Tamper Evident foil seal not completely intact.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 15, 2018. Severity: Moderate. Recall number: D-1042-2018.
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