FindMyRecallSubscribe
Class III: unlikely to cause harmTerminated

West-Ward Columbus Doxercalciferol Capsules 0 Recall

Doxercalciferol Capsules 0

West-Ward Columbus, Inc. · Columbus, OH

Risk level
Class III
Reported by FDA
Apr 19, 2017
Recall ID
D-0651-2017
Check your lot numberHow we source this data

Summary

West-Ward Columbus recalled Doxercalciferol Capsules 0 starting Apr 4, 2017. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0651-2017 on Apr 19, 2017. Reason: Failed Tablet/Capsule Specifications; during an internal inspection, capsules were found with illegible print. Status: Terminated.

Why it was recalled

Failed Tablet/Capsule Specifications; during an internal inspection, capsules were found with illegible print.

Product description

Doxercalciferol Capsules 0.5mcg, 50 count bottles, Rx, only, Manufactured by Cipla Limited Kurkumbh, Maharashtra, India, Manufactured for West-Ward, Pharmaceuticals, Corp., Eatontown, NJ -- NDC 0054-0338-19

Lot numbers, UPCs & expiration codes

Lot KB60707, 10/31/2018

Where it was sold

The recalled product was distributed to the following state: OH. There are no Canada accounts for this recall. There are no Mexico accounts for this recall. There are no government accounts for this recall.

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-0651-2017
Classification
Class III
Status
Terminated
Recall initiated
Apr 4, 2017
FDA report date
Apr 19, 2017
Quantity
100 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
West-Ward Columbus, Inc.

Original FDA data

Every field from FDA enforcement report D-0651-2017, exactly as published.

Show all FDA fields
City
Columbus
State
OH
Status
Terminated
Country
United States
Event ID
76822
Address
1809 Wilson Rd
Code information
Lot KB60707, 10/31/2018
Postal code
43228-9579
Report date
Apr 19, 2017
Product type
Drugs
Recall number
D-0651-2017
Classification
Class III
Recalling firm
West-Ward Columbus, Inc.
Product quantity
100 bottles
Termination date
Sep 4, 2018
Reason for recall
Failed Tablet/Capsule Specifications; during an internal inspection, capsules were found with illegible print.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Doxercalciferol Capsules 0.5mcg, 50 count bottles, Rx, only, Manufactured by Cipla Limited Kurkumbh, Maharashtra, India, Manufactured for West-Ward, Pharmaceuticals, Corp., Eatontown, NJ -- NDC 0054-0338-19
Distribution pattern
The recalled product was distributed to the following state: OH. There are no Canada accounts for this recall. There are no Mexico accounts for this recall. There are no government accounts for this recall.
Recall initiation date
Apr 4, 2017
Initial firm notification
Letter
Center classification date
Apr 7, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0651-2017, published Apr 19, 2017. 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