US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Oct 17, 2025 (11 months ago)

Acetaminophen 500mg Caffeine 65mg caplets, packaged as 2 caplets per packet further…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Labeling: Label Mix-up. This issue affects the outer box labeling only. The box incorrectly states the ingredients Acetaminophen 500mg and Caffeine 65mg. The inner pouch correctly states the ingredients are Aspirin (NSAID)*500mg and Caffeine 32.5mg.

What was recalled

Acetaminophen 500mg Caffeine 65mg caplets, packaged as 2 caplets per packet further packaged in a 50-count box, AERO TAB, Manufactured for AERO HEALTHCARE US, Valley-Cottage, NY, 10989, NDC 55305-135-01

Recalling firm
Aero Healthcare
NDC code
55305-135-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0155-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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