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Class II: temporary or reversible health riskTerminated

Cardinal Healthcare Warfarin Sodium Tablets Recall

Warfarin Sodium Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for:…

CARDINAL HEALTHCARE · Dublin, OH

Risk level
Class II
Reported by FDA
Jan 3, 2024
Recall ID
D-0201-2024
Check your lot numberHow we source this data

Summary

Cardinal Healthcare recalled Warfarin Sodium Tablets starting Jan 26, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0201-2024 on Jan 3, 2024. Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions. Status: Terminated.

Why it was recalled

CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.

Product description

Warfarin Sodium Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 0093-1721-01

Lot numbers, UPCs & expiration codes

Batch 2323041

Where it was sold

Nationwide USA

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-0201-2024
Classification
Class II
Status
Terminated
Recall initiated
Jan 26, 2022
FDA report date
Jan 3, 2024
Quantity
1 unit
Recall type
Voluntary: Firm initiated
Recalling firm
CARDINAL HEALTHCARE

Original FDA data

Every field from FDA enforcement report D-0201-2024, exactly as published.

Show all FDA fields
City
Dublin
State
OH
Status
Terminated
Country
United States
Event ID
89450
Address
7200 Cardinal Pl W
Code information
Batch 2323041
Postal code
43017-1094
Report date
Jan 3, 2024
Product type
Drugs
Recall number
D-0201-2024
Classification
Class II
Recalling firm
CARDINAL HEALTHCARE
Product quantity
1 unit
Termination date
Sep 29, 2024
Reason for recall
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Warfarin Sodium Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 0093-1721-01
Distribution pattern
Nationwide USA
Recall initiation date
Jan 26, 2022
Initial firm notification
Letter
Center classification date
Dec 26, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0201-2024, published Jan 3, 2024. 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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