Morton Grove Pharmaceuticals, Inc.

FDA recalling firm · 7 enforcement events · 9 product records · 2015–2022 · IL

Morton Grove Pharmaceuticals, Inc. has 7 FDA enforcement events on this register (9 product records) between 2015 and 2022: 7 drug; the busiest year was 2015 with 1.

0% of its events are Class I; the most common class is Class II (6). 0 events are listed as ongoing; the recalling firm's address is in IL.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
21 Feb 2022	Dexamethasone Elixir, USP 0.5 mg/5 mL, Net: 8 fl oz (237 mL) bottle, Rx only, Manufactured By: Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053, NDC 60432-466-08.	Drug	Class II	1	Terminated
3 Sep 2021	Promethazine Syrup Plain, 6.25 mg/5 mL (Promethazine Hydrochloride Syrup, USP), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-608-16	Drug	Class II	3	Completed
9 Dec 2020	Hydroxyzine Hydrochloride Oral Solution, USP (Syrup), 10 mg/5 mL, packaged in a) 4 fl oz (118 mL) bottle, NDC 60432-150-04, b) 1 pint (473 mL), NDC 60432-150-16, Rx Only, Manufactured By: Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053	Drug	Class II	1	Terminated
23 Sep 2019	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	Drug	Class II	1	Terminated
24 Jul 2018	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.	Drug	Class II	1	Terminated
10 Aug 2017	Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted) bottle, Rx Only, Manufactured By: Cipla Ltd. at Medispray Laboratories Pvt. Ltd., Kundaim Goa, India; Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054, NDC 60432-065-00.	Drug	Class II	1	Terminated
15 Dec 2015	Lindane Lotion, USP 1%, For External use Only, Rx Only, 2 fl oz (60 mL) bottle, MGP, NDC 60432-833-60	Drug	Class III	1	Terminated

By type and class

Drug7

Class II6

Class III1

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Morton Grove Pharmaceuticals, Inc. by year initiated.

Questions and answers

How many FDA recalls has Morton Grove Pharmaceuticals, Inc. had?

7 enforcement events (9 product records) on this register, 2015–2022: 7 drug.

Are any Morton Grove Pharmaceuticals, Inc. recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Morton Grove Pharmaceuticals, Inc. recalls?

6 Class II, 1 Class III. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.