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Class IOngoing

Healthy Living Acetaminophen recall

FDA recall D-0641-2024 · initiated Jul 11, 2024

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Aug 28, 2024How we research

Aurobindo Pharma USA Inc recalled Healthy Living Acetaminophen in Jul 2024 — an FDA Class I recall (D-0641-2024) because Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.

Most serious — a reasonable probability that use will cause serious harm or death.

Why it was recalled

Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.

Labelling, packaging or a product mix-up

The wrong information — or the wrong medicine — ended up in the pack. A mix-up is a manufacturing failure that can still be dangerous to swallow.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot#: AC2523005A, Exp 6/30/2025

Quantity recalled: 240 bottles

Details

Product
Healthy Living Acetaminophen, Aspirin (NSAID) and Caffeine, tablets USP, 250 mg/250 mg/65 mg, 100-count bottles, Distributed by: Aurohealth LLC, 279 Princeton-Hightstown Road, East Windsor, NJ , Made in India, NDC 58602-882-21.
Recalling company
Aurobindo Pharma Limited
Classification
Class I
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
NJ, NY & PA
Initiated
Jul 11, 2024
FDA report date
Aug 28, 2024
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Healthy Living Acetaminophen recalled?
Aurobindo Pharma USA Inc recalled Healthy Living Acetaminophen in Jul 2024 — an FDA Class I recall (D-0641-2024) because Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information. Most serious — a reasonable probability that use will cause serious harm or death.
Why was Healthy Living Acetaminophen recalled?
Per the FDA enforcement record, the reason for recall D-0641-2024 was: Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.
Is a recalled Healthy Living Acetaminophen dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Most serious — a reasonable probability that use will cause serious harm or death. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Healthy Living Acetaminophen are affected?
Distributed: NJ, NY & PA. The recall covers these lots — Lot#: AC2523005A, Exp 6/30/2025. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0641-2024.

Source: openFDA Drug Enforcement record D-0641-2024

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