Home / Brands / Morton Grove Pharmaceuticals
Morton Grove Pharmaceuticals Recalls
9 recalls on record · January 27, 2016 to March 9, 2022 · Drugs
Recalls by year
16
17
18
19
20
21
22
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 9, 2022DrugsFDA
Morton Grove Pharmaceuticals, Inc. recalls Dexamethasone Elixir, USP 0.5 mg/5 mL, Net: 8 fl oz (237 mL) bottle, Rx only, Manufactured By: Morton Grove Pharmaceutic
Hazard: Failed Impurities/Degradation Specifications: higher than permissible levels of unknown impurities were found in the drug product.
September 29, 2021DrugsFDA
Morton Grove Pharmaceuticals, Inc. recalls Valproic Acid Oral Solution USP, (250 mg/5 mL), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsip
Hazard: CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
September 29, 2021DrugsFDA
Morton Grove Pharmaceuticals, Inc. recalls Promethazine With Codeine Oral Solution, (Promethazine Hydrochloride 6.25 mg/5mL & Codeine Phosphate 10 mg/5 mL), 1 Pint
Hazard: CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
September 29, 2021DrugsFDA
Morton Grove Pharmaceuticals, Inc. recalls Promethazine Syrup Plain, 6.25 mg/5 mL (Promethazine Hydrochloride Syrup, USP), 1 Pint (473 mL), Rx Only, Manufactured F
Hazard: CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
December 30, 2020DrugsFDA
Morton Grove Pharmaceuticals, Inc. recalls Hydroxyzine Hydrochloride Oral Solution, USP (Syrup), 10 mg/5 mL, packaged in a) 4 fl oz (118 mL) bottle, NDC 60432-150-
Hazard: Failed Impurities/Degradation Specification: OOS for the following - unknown degradant/impurity, 4-chorobenzophenone, and for total impurities.
October 16, 2019DrugsFDA
Morton Grove Pharmaceuticals, Inc. recalls Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, packaged in a 8 fl oz (237 mL) bottle, Rx only, Manufactured By
Hazard: Failed Impurities/Degradation Specifications - failed specs for Prednisolone Impurity 14
August 15, 2018DrugsFDA
Morton Grove Pharmaceuticals, Inc. recalls Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, 8 fl oz (237 mL) Bottle, Rx only, Manufactured By: Morton Grov
Hazard: Defective Container: Tamper Evident foil seal not completely intact.
September 6, 2017DrugsFDA
Morton Grove Pharmaceuticals, Inc. recalls Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted) bottle
Hazard: Presence of Foreign Substance: customer complaint of blue foreign material identified as a portion of a nitrile glove was discovered in product.
January 27, 2016DrugsFDA
Morton Grove Pharmaceuticals, Inc. recalls Lindane Lotion, USP 1%, For External use Only, Rx Only, 2 fl oz (60 mL) bottle, MGP, NDC 60432-833-60
Hazard: Super-Potent Drug: Out of Specification Assay test results were reported for stability samples.