Aurobindo Pharma USA Inc recalls Healthy Living Acetaminophen, Aspirin (NSAID) and Caffeine, tablets USP, 250 mg/250 mg/65 mg, 100-count bottles,
Aurobindo Pharma recalls 100-count Healthy Living Acetaminophen, Aspirin and Caffeine tablets due to missing manufacturer label. This affects some bottles sold in the US with specific lot numbers.
Lower-risk recall
Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.
Contact the company & request your remedy
What happened, in plain English
Aurobindo Pharma is recalling 100-count Healthy Living Acetaminophen, Aspirin and Caffeine tablets because some bottles lack the required manufacturer label. This recall is important because the missing label makes it difficult to verify the product's contents and safety. Read more at govinfonow.com/recall/32589-healthy-living-acetaminophen-tablets-recall-missing-manufacturer-label.
Source Summary by GovInfoNow · govinfonow.com/recall/32589-healthy-living-acetaminophen-tablets-recall-missing-manufacturer-label · Updated September 23, 2026 · FDA enforcement record: FDA #D-0641-2024
Cite this page
“Healthy Living Acetaminophen Tablets Recall: Missing Manufacturer Label.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32589-healthy-living-acetaminophen-tablets-recall-missing-manufacturer-label. Based on FDA recall #D-0641-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0641-2024%22&limit=1).
Why it’s dangerous
The product lacks the required manufacturer label that includes drug facts information. Without this label, users cannot confirm the product's contents or safety, which could lead to confusion about the medication being taken.
Who’s affected
People who own or use the recalled 100-count Healthy Living Acetaminophen, Aspirin and Caffeine tablets with the specific lot number AC2523005A are affected. Those who have the product without the label are at slightly higher risk of confusion.
How to tell if you have this one
Check for the label with the manufacturer information on the bottle. The recalled product has the lot number AC2523005A and was distributed by Aurohealth LLC in the US.
- Brand
Aurobindo Pharma- Category
Drug
What to do — step by step
Check Label
Look for the manufacturer label that includes drug facts information on the bottle.
Questions people ask
Why is this product being recalled?
The product is being recalled because some bottles are missing the required manufacturer label that includes drug facts information.
What should I do if I have the recalled product?
The official recall notice does not specify a remedy for this product, so no action is required beyond checking the label.
Is this product safe to use?
The product may be safe to use, but the missing label makes it difficult to verify the contents and safety.
Contact Aurobindo Pharma
We’ve drafted a message you can send Aurobindo Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0641-2024 — Aurobindo Pharma Aurobindo Pharma Hello, I own a Aurobindo Pharma that is covered by recall D-0641-2024 from Aurobindo Pharma. 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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Where this comes from
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.
- Official source: FDA Recall #D-0641-2024 (July 11, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0641-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.