Aero Healthcare recalls 50-count boxes of Acetaminophen 500mg Caffeine 65mg caplets due to outer box labeling error. The inner pouch correctly lists Aspirin 500mg and Caffeine 32.5mg.
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.
Aero Healthcare is recalling 50-count boxes of acetaminophen/caffeine caplets because the outer box incorrectly lists the ingredients. This mix-up only affects labeling, not the actual contents inside the pouch.
The outer box incorrectly states the product contains acetaminophen 500mg and caffeine 65mg. The inner pouch correctly lists aspirin 500mg and caffeine 32.5mg. This labeling mix-up could lead to confusion about the actual ingredients.
People who bought the 50-count boxes of Aero Healthcare acetaminophen/caffeine caplets between the specified lots. Those using the product for pain or headaches are most at risk if they rely on the outer box label.
Check for the 50-count box labeled 'AERO TAB' with lot numbers 9282 (expiring September 2026) or 9310 (expiring November 2026). The inner pouch shows aspirin 500mg and caffeine 32.5mg.
Look inside the pouch for the correct ingredients: Aspirin 500mg and Caffeine 32.5mg.
No, the labeling mix-up only affects the outer box. The actual contents inside the pouch are correct and safe.
No, you can continue using it as the inner pouch has the correct ingredients. The issue is only with the outer box label.
Check for the 50-count box labeled 'AERO TAB' with lot numbers 9282 (expiring September 2026) or 9310 (expiring November 2026).
We’ve drafted a message you can send Aero Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0155-2026 — Aero Healthcare Aero Healthcare Hello, I own a Aero Healthcare that is covered by recall D-0155-2026 from Aero Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
