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Class II: temporary or reversible health riskTerminated

Dr. Reddy's Metoprolol Succinate Recall

Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Onl…

Dr. Reddy's Laboratories, Inc. · Princeton, NJ

Risk level
Class II
Reported by FDA
Feb 12, 2014
Recall ID
D-1080-2014
Check your lot numberHow we source this data

Summary

Dr. Reddy's Laboratories recalled Dr. Reddy's Metoprolol Succinate starting Dec 13, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1080-2014 on Feb 12, 2014. Reason: Failed Dissolution Specification; 12-Month stability interval. Status: Terminated.

Why it was recalled

Failed Dissolution Specification; 12-Month stability interval.

Product description

Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd. By: Dr. Reddy's Laboratories Limited Bachepalli -500 090 INDIA NDC 55111-467-01

Lot numbers, UPCs & expiration codes

Lot # C207420 and C207416

Where it was sold

LA, MI, MO, MS & OH

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-1080-2014
Classification
Class II
Status
Terminated
Recall initiated
Dec 13, 2013
FDA report date
Feb 12, 2014
Quantity
8,592 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Dr. Reddy's Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-1080-2014, exactly as published.

Show all FDA fields
City
Princeton
State
NJ
Status
Terminated
Country
United States
Event ID
67293
Address
107 College Rd E
Code information
Lot # C207420 and C207416
Postal code
08540-6623
Report date
Feb 12, 2014
Product type
Drugs
Recall number
D-1080-2014
Classification
Class II
Recalling firm
Dr. Reddy's Laboratories, Inc.
Product quantity
8,592 bottles
Termination date
Feb 12, 2015
Reason for recall
Failed Dissolution Specification; 12-Month stability interval.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd. By: Dr. Reddy's Laboratories Limited Bachepalli -500 090 INDIA NDC 55111-467-01
Distribution pattern
LA, MI, MO, MS & OH
Recall initiation date
Dec 13, 2013
Initial firm notification
Letter
Center classification date
Feb 6, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1080-2014, published Feb 12, 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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