CLASS III Drug recall · Reported 14 Aug 2019 · FDA Enforcement Report
Smart Sense Regular Strength Aspirin Tablets, 325 mg recalled
AAA Pharmaceutical is recalling Smart Sense Regular Strength Aspirin Tablets, 325 mg, distributed in Kansas. The recall was initiated on 25 Jun 2019 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-1585-2019
- FDA event ID
- 83210
- Recalling firm
- AAA Pharmaceutical, Lumberton, NJ
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 25 Jun 2019
- FDA classified
- 2 Aug 2019
- Reported
- 14 Aug 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Drug class
- Pain Medication
Timeline
| 25 Jun 2019 | Recall initiated by company | |
| 2 Aug 2019 | Classified by FDA | +38 days |
| 14 Aug 2019 | Published in enforcement report | +12 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 Number and/or Exp Date; Product has an incorrect expiration date of 9/2022 applied to the labeling, where the actual expiration date is 10/2021.
Product as listed by the FDA
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
Where it was distributed
KS
Questions about this recall
Why was it recalled?
Labeling; Incorrect or Missing Lot Number and/or Exp Date; Product has an incorrect expiration date of 9/2022 applied to the labeling, where the actual expiration date is 10/2021.
Which lots are affected?
a) P136370, exp 9/2022 b) P136366, exp 9/2022
Where was it sold?
KS
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.
More recalls from AAA Pharmaceutical
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Discount Drug Mart, Allergy Relief recalled by AAA Pharmaceutical | AAA Pharmaceutical | Other | OH |
| 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 |