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Class III: unlikely to cause harmOngoing

Akron Pharma Acetaminophen Extra Strength 500 mg Recall

Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc

Akron Pharma, Inc. · Fairfield, NJ

Risk level
Class III
Reported by FDA
Jan 22, 2025
Recall ID
D-0193-2025
Check your lot numberHow we source this data

Summary

Akron Pharma recalled Acetaminophen Extra Strength 500 mg starting Dec 12, 2024. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0193-2025 on Jan 22, 2025. Reason: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. Status: Ongoing.

Why it was recalled

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Product description

Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.

Lot numbers, UPCs & expiration codes

Lot: KDT0224002A, Exp 09/30/2026

Where it was sold

Nationwide in the US

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0193-2025
Classification
Class III
Status
Ongoing
Recall initiated
Dec 12, 2024
FDA report date
Jan 22, 2025
Quantity
768 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Akron Pharma, Inc.

Original FDA data

Every field from FDA enforcement report D-0193-2025, exactly as published.

Show all FDA fields
City
Fairfield
State
NJ
Status
Ongoing
Country
United States
Event ID
95944
Address
373 Us Highway 46 Ste 117
Code information
Lot: KDT0224002A, Exp 09/30/2026
Postal code
07004-2456
Report date
Jan 22, 2025
Product type
Drugs
Recall number
D-0193-2025
Classification
Class III
Recalling firm
Akron Pharma, Inc.
Product quantity
768 bottles
Reason for recall
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.
Distribution pattern
Nationwide in the US
Recall initiation date
Dec 12, 2024
Initial firm notification
Letter
Center classification date
Jan 10, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0193-2025, published Jan 22, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

How we source and update recall data · Report incorrect information

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