CLASS III Drug recall · Reported 11 Mar 2020 · FDA Enforcement Report
Discount Drug Mart, Allergy Relief recalled by AAA Pharmaceutical
AAA Pharmaceutical is recalling Discount Drug Mart, Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, distributed in Ohio. The recall was initiated on 14 Feb 2020 and the FDA has classified it as Class III.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0868-2020
- FDA event ID
- 84938
- Recalling firm
- AAA Pharmaceutical, Lumberton, NJ
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 14 Feb 2020
- FDA classified
- 4 Mar 2020
- Reported
- 11 Mar 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Drug class
- Allergy Medication
Timeline
| 14 Feb 2020 | Recall initiated by company | |
| 4 Mar 2020 | Classified by FDA | +19 days |
| 11 Mar 2020 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Incorrect or Missing Lot and/or Expiration date.
Product as listed by the FDA
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 Commerce Drive, Medina, OH 44256.
Where it was distributed
Ohio
Questions about this recall
Why was it recalled?
Labeling: Incorrect or Missing Lot and/or Expiration date.
Which lots are affected?
Lot #s: a) P138855, Exp. 05/30/2022; b) P138856, Exp. 05/30/2022
Where was it sold?
Ohio
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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|---|---|---|---|---|---|
| Drug | CLASS II | Ranitidine 150 mg tablets, 130 count bottles recalled | AAA Pharmaceutical | Nitrosamine Impurity | NJ |
| Drug | CLASS II | Ranitidine 150 mg tablets, 24 count bottles recalled | AAA Pharmaceutical | Nitrosamine Impurity | NJ |
| Drug | CLASS III | Smart Sense Regular Strength Aspirin Tablets, 325 mg recalled | AAA Pharmaceutical | Other | KS |
Other Discount Drug Mart recalls
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Discount drug mart, Extra Strength, Antacid Tablets recalled | Guardian Drug | Particulate Matter | Nationwide |
| Drug | CLASS II | Discount Drug Mart, Food Fair, Saline Nasal Spray recalled | Product Quest Manufacturing | Manufacturing (CGMP) Deviations | Nationwide |