FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

Sun Pharma Global Fze Levetiracetam Recall

Levetiracetam, extended release tablets, 750 mg, 60-count bottle, Rx only, Manufactured…

Sun Pharma Global Fze · Sharm, N/A

Risk level
Class II
Reported by FDA
Feb 18, 2015
Recall ID
D-0386-2015
Check your lot numberHow we source this data

Summary

Sun Pharma Global Fze recalled Levetiracetam starting Jan 21, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0386-2015 on Feb 18, 2015. Reason: Failed Dissolution Specifications: 6 month time point. Status: Terminated.

Why it was recalled

Failed Dissolution Specifications: 6 month time point.

Product description

Levetiracetam, extended release tablets, 750 mg, 60-count bottle, Rx only, Manufactured by Sun Pharmaceutical Ind. Ltd Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC Number: 47335-576-86

Lot numbers, UPCs & expiration codes

Lot #: JKN0249A Exp 02/2016

Where it was sold

Nationwide.

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-0386-2015
Classification
Class II
Status
Terminated
Recall initiated
Jan 21, 2015
FDA report date
Feb 18, 2015
Quantity
3263 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Sun Pharma Global Fze

Original FDA data

Every field from FDA enforcement report D-0386-2015, exactly as published.

Show all FDA fields
City
Sharm
Status
Terminated
Country
United Arab Emirates
Event ID
70339
Address
Office # 43 Block Y Saif Zone
Code information
Lot #: JKN0249A Exp 02/2016
Report date
Feb 18, 2015
Product type
Drugs
Recall number
D-0386-2015
Classification
Class II
Recalling firm
Sun Pharma Global Fze
Product quantity
3263 bottles
Termination date
Oct 23, 2015
Reason for recall
Failed Dissolution Specifications: 6 month time point.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Levetiracetam, extended release tablets, 750 mg, 60-count bottle, Rx only, Manufactured by Sun Pharmaceutical Ind. Ltd Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC Number: 47335-576-86
Distribution pattern
Nationwide.
Recall initiation date
Jan 21, 2015
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Feb 12, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0386-2015, published Feb 18, 2015. 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

Other recent drug recalls