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Class II: temporary or reversible health riskTerminated

Watson Laboratories Meprobamate Recall

Meprobamate, Tablets USP, 200 mg, 100 tablets

Watson Laboratories Inc · Corona, CA

Risk level
Class II
Reported by FDA
Mar 27, 2013
Recall ID
D-203-2013
Check your lot numberHow we source this data

Summary

Watson Laboratories recalled Meprobamate starting Feb 8, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-203-2013 on Mar 27, 2013. Reason: Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is recalling meprobamate because an out of specification result for an impurity diphenyl sulfone . Status: Terminated.

Why it was recalled

Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is recalling meprobamate because an out of specification result for an impurity diphenyl sulfone .

Product description

Meprobamate, Tablets USP, 200 mg, 100 tablets; Rx only; Manufactured By: Watson Laboratories, Inc., Corona, CA 92800 USA; 173266; . Distributed by: Watson Pharma, Inc., NDC 9591-5239-01

Lot numbers, UPCs & expiration codes

386585A, Exp. 02/13; 429104A, Exp. 06/13; 474487A, Exp. 11/13; 491671A, Exp.01/14.

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-203-2013
Classification
Class II
Status
Terminated
Recall initiated
Feb 8, 2013
FDA report date
Mar 27, 2013
Quantity
9,824 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Watson Laboratories Inc

Original FDA data

Every field from FDA enforcement report D-203-2013, exactly as published.

Show all FDA fields
City
Corona
State
CA
Status
Terminated
Country
United States
Event ID
64312
Address
311 Bonnie Cir
Code information
386585A, Exp. 02/13; 429104A, Exp. 06/13; 474487A, Exp. 11/13; 491671A, Exp.01/14.
Postal code
92880-2882
Report date
Mar 27, 2013
Product type
Drugs
Recall number
D-203-2013
Classification
Class II
Recalling firm
Watson Laboratories Inc
Product quantity
9,824 bottles
Termination date
Jan 31, 2014
Reason for recall
Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is recalling meprobamate because an out of specification result for an impurity diphenyl sulfone .
Voluntary / mandated
Voluntary: Firm initiated
Product description
Meprobamate, Tablets USP, 200 mg, 100 tablets; Rx only; Manufactured By: Watson Laboratories, Inc., Corona, CA 92800 USA; 173266; . Distributed by: Watson Pharma, Inc., NDC 9591-5239-01
Distribution pattern
Nationwide and Puerto Rico
Recall initiation date
Feb 8, 2013
Initial firm notification
Letter
Center classification date
Mar 19, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-203-2013, published Mar 27, 2013. 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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