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Class I: serious health riskTerminated

American Health Packaging Oxcarbazepine Tablets Recall

Oxcarbazepine Tablets, 300 mg, 100 tablets per carton (10 x 10), Rx Only, Packaged and…

American Health Packaging · Columbus, OH

Risk level
Class I
Reported by FDA
Sep 24, 2014
Recall ID
D-1590-2014
Check your lot numberHow we source this data

Summary

American Health Packaging recalled Oxcarbazepine Tablets starting Jul 1, 2014. The FDA classified it as Class I (serious health risk) and published enforcement report D-1590-2014 on Sep 24, 2014. Reason: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg, lot #142588 that contain blister cards filled with Ibuprofen tablets, 600mg drug product, were found to be mis-labeled with blister card print identifying the product as AHP Oxcarbazepine Tablets, 300mg, lot #142544. Status: Terminated.

Why it was recalled

Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg, lot #142588 that contain blister cards filled with Ibuprofen tablets, 600mg drug product, were found to be mis-labeled with blister card print identifying the product as AHP Oxcarbazepine Tablets, 300mg, lot #142544.

Product description

Oxcarbazepine Tablets, 300 mg, 100 tablets per carton (10 x 10), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, OH 43217, NDC 62584-143-01

Lot numbers, UPCs & expiration codes

Lot #142544, Exp 02/2016

Where it was sold

Nationwide and Puerto Rico

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-1590-2014
Classification
Class I
Status
Terminated
Recall initiated
Jul 1, 2014
FDA report date
Sep 24, 2014
Quantity
59,200 tablets
Recall type
Voluntary: Firm initiated
Recalling firm
American Health Packaging

Original FDA data

Every field from FDA enforcement report D-1590-2014, exactly as published.

Show all FDA fields
City
Columbus
State
OH
Status
Terminated
Country
United States
Event ID
68779
Address
2550 John Glenn Ave
Address (line 2)
Suite A
Code information
Lot #142544, Exp 02/2016
Postal code
43217-1188
Report date
Sep 24, 2014
Product type
Drugs
Recall number
D-1590-2014
Classification
Class I
Recalling firm
American Health Packaging
Product quantity
59,200 tablets
Termination date
Aug 3, 2015
Reason for recall
Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg, lot #142588 that contain blister cards filled with Ibuprofen tablets, 600mg drug product, were found to be mis-labeled with blister card print identifying the product as AHP Oxcarbazepine Tablets, 300mg, lot #142544.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Oxcarbazepine Tablets, 300 mg, 100 tablets per carton (10 x 10), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, OH 43217, NDC 62584-143-01
Distribution pattern
Nationwide and Puerto Rico
Recall initiation date
Jul 1, 2014
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Sep 18, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1590-2014, published Sep 24, 2014. 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.

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