AAA Pharmaceutical, Inc.
AAA Pharmaceutical, Inc. has 3 FDA enforcement events on this register (4 product records) between 2019 and 2020: 3 drug; the busiest year was 2019 with 2.
0% of its events are Class I; the most common class is Class III (2). 0 events are listed as ongoing; the recalling firm's address is in NJ.
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 |
|---|---|---|---|---|---|
| 14 Feb 2020 | Discount Drug Mart, Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg /Antihistamine, Indoor/Outdoor Allergies, 24 Hour, a) 30 tablets per bottle, NDC 53943-192-04, UPC Code 0-93351-03069-7; b) 45 tablets per bottle, NDC 53943-192-06, UPC Code 0-93351-03070-3, Distributed by: Drug Mart -Food Fair, 211… | Drug | Class III | 1 | Terminated |
| 26 Dec 2019 | Ranitidine 150 mg tablets, 24 count bottles, NDC 37808-196-01. | Drug | Class II | 2 | Terminated |
| 25 Jun 2019 | Smart Sense Regular Strength Aspirin Tablets, 325 mg packed in a) 100 count UPC 8-8397-38781-6 and b) 500 count UPC 8-83967-38786-1 bottles, Distributed by: Kmart Corporation Hoffman Estates, IL 60179 | Drug | Class III | 1 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has AAA Pharmaceutical, Inc. had?
3 enforcement events (4 product records) on this register, 2019–2020: 3 drug.
Are any AAA Pharmaceutical, Inc. recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are AAA Pharmaceutical, Inc. recalls?
2 Class III, 1 Class II. 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.