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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 83210

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 25, 2019
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
AAA Pharmaceutical, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

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

D-1585-2019
Recall number
D-1585-2019
Initiated
June 25, 2019
Classification
Class III
Status
Terminated
Recalling firm
AAA Pharmaceutical, Inc.
Quantity
a) 288 bottles b) 48 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Labeling; Incorrect or Missing

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

a) P136370, exp 9/2022 b) P136366, exp 9/2022

Distribution pattern

KS