FindMyRecallSubscribe
Class III: unlikely to cause harmTerminated

Dr. Reddy's Laboratories Paricalcitol Capsules Recall

Paricalcitol Capsules, 2 mcg, 30 capsules per bottle, Rx Only, Mfd by: Dr

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

Risk level
Class III
Reported by FDA
Feb 24, 2016
Recall ID
D-0720-2016
Check your lot numberHow we source this data

Summary

Dr. Reddy's Laboratories recalled Paricalcitol Capsules starting Nov 4, 2015. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0720-2016 on Feb 24, 2016. Reason: Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules. Status: Terminated.

Why it was recalled

Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules.

Product description

Paricalcitol Capsules, 2 mcg, 30 capsules per bottle, Rx Only, Mfd by: Dr. Reddy's Laboratories Limited, Bachupally, India, NDC 55111-664-30

Lot numbers, UPCs & expiration codes

Lot #s: C404653, C404654, C404655, Exp 05/2016; C505010, Exp 06/2017

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-0720-2016
Classification
Class III
Status
Terminated
Recall initiated
Nov 4, 2015
FDA report date
Feb 24, 2016
Quantity
4383 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Dr. Reddy's Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-0720-2016, exactly as published.

Show all FDA fields
City
Princeton
State
NJ
Status
Terminated
Country
United States
Event ID
72648
Address
107 College Rd E
Code information
Lot #s: C404653, C404654, C404655, Exp 05/2016; C505010, Exp 06/2017
Postal code
08540-6623
Report date
Feb 24, 2016
Product type
Drugs
Recall number
D-0720-2016
Classification
Class III
Recalling firm
Dr. Reddy's Laboratories, Inc.
Product quantity
4383 bottles
Termination date
Jun 22, 2017
Reason for recall
Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Paricalcitol Capsules, 2 mcg, 30 capsules per bottle, Rx Only, Mfd by: Dr. Reddy's Laboratories Limited, Bachupally, India, NDC 55111-664-30
Distribution pattern
Nationwide
Recall initiation date
Nov 4, 2015
Initial firm notification
Letter
Center classification date
Feb 18, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0720-2016, published Feb 24, 2016. 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