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Class II: temporary or reversible health riskTerminated

Wockhardt Lansoprazole Delayed-Release Capsules Recall

Lansoprazole Delayed-Release Capsules, USP, 15 mg Capsules, For Repackaging Only, Packa…

Wockhardt Usa Inc. · Parsippany, NJ

Risk level
Class II
Reported by FDA
Jul 29, 2015
Recall ID
D-1251-2015
Check your lot numberHow we source this data

Summary

Wockhardt recalled Lansoprazole Delayed-Release Capsules starting Apr 22, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1251-2015 on Jul 29, 2015. Reason: CGMP Deviations: Firm did not adequately investigate customer complaints. Status: Terminated.

Why it was recalled

CGMP Deviations: Firm did not adequately investigate customer complaints.

Product description

Lansoprazole Delayed-Release Capsules, USP, 15 mg Capsules, For Repackaging Only, Packaged in 4500 Count Pouches, Over the Counter. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA. NDC: 64679-140-00.

Lot numbers, UPCs & expiration codes

Lot #: LN11086, Expiry: 5/31/2015.

Where it was sold

U.S. Nationwide including 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-1251-2015
Classification
Class II
Status
Terminated
Recall initiated
Apr 22, 2015
FDA report date
Jul 29, 2015
Quantity
848 Pouches
Recall type
Voluntary: Firm initiated
Recalling firm
Wockhardt Usa Inc.

Original FDA data

Every field from FDA enforcement report D-1251-2015, exactly as published.

Show all FDA fields
City
Parsippany
State
NJ
Status
Terminated
Country
United States
Event ID
71104
Address
20 Waterview Blvd Ste 3
Code information
Lot #: LN11086, Expiry: 5/31/2015.
Postal code
07054-1271
Report date
Jul 29, 2015
Product type
Drugs
Recall number
D-1251-2015
Classification
Class II
Recalling firm
Wockhardt Usa Inc.
Product quantity
848 Pouches
Termination date
May 9, 2018
Reason for recall
CGMP Deviations: Firm did not adequately investigate customer complaints.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Lansoprazole Delayed-Release Capsules, USP, 15 mg Capsules, For Repackaging Only, Packaged in 4500 Count Pouches, Over the Counter. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA. NDC: 64679-140-00.
Distribution pattern
U.S. Nationwide including Puerto Rico.
Recall initiation date
Apr 22, 2015
Initial firm notification
Letter
Center classification date
Jul 17, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1251-2015, published Jul 29, 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.

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