July 2018 FDA Recall Drug by Morton Grove Pharmaceuticals, Inc.
D-1042-2018 - Defective Container

This Class II drug recall was voluntarily initiated by Morton Grove Pharmaceuticals, Inc. on July 24, 2018 for the product Drug. The FDA reported the reason for recall as defective container. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-1042-2018

Reason for Recall
Defective Container: Tamper Evident foil seal not completely intact.
Initiated
07-24-2018
Reported
08-15-2018
Quantity
38,280 bottles

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Morton Grove Pharmaceuticals, Inc.
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.

Batch or Lot Expiration Information

Lot# Lot US1259