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Class II: temporary or reversible health riskTerminated

Sandoz Isosorbide Dinitrate Tablets Recall

Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sand…

Sandoz Inc · Princeton, NJ

Risk level
Class II
Reported by FDA
Nov 21, 2018
Recall ID
D-0259-2019
Check your lot numberHow we source this data

Summary

Sandoz recalled Isosorbide Dinitrate Tablets starting Nov 2, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0259-2019 on Nov 21, 2018. Reason: Cross Contamination with Other Products. Status: Terminated.

Why it was recalled

Cross Contamination with Other Products

Product description

Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-223-00

Lot numbers, UPCs & expiration codes

Lot #: HZ7896, Exp. 05/2021

Where it was sold

Nationwide within the United States

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-0259-2019
Classification
Class II
Status
Terminated
Recall initiated
Nov 2, 2018
FDA report date
Nov 21, 2018
Quantity
7817 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Sandoz Inc

Original FDA data

Every field from FDA enforcement report D-0259-2019, exactly as published.

Show all FDA fields
City
Princeton
State
NJ
Status
Terminated
Country
United States
Event ID
81457
Address
100 College Rd W
Code information
Lot #: HZ7896, Exp. 05/2021
Postal code
08540-6604
Report date
Nov 21, 2018
Product type
Drugs
Recall number
D-0259-2019
Classification
Class II
Recalling firm
Sandoz Inc
Product quantity
7817 bottles
Termination date
Oct 2, 2020
Reason for recall
Cross Contamination with Other Products
Voluntary / mandated
Voluntary: Firm initiated
Product description
Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-223-00
Distribution pattern
Nationwide within the United States
Recall initiation date
Nov 2, 2018
Initial firm notification
Letter
Center classification date
Nov 20, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0259-2019, published Nov 21, 2018. 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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