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Class III: unlikely to cause harmTerminated

Alvogen Adalat CC Recall

Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Man…

Alvogen, Inc · Pine Brook, NJ

Risk level
Class III
Reported by FDA
Apr 12, 2017
Recall ID
D-0635-2017
Check your lot numberHow we source this data

Summary

Alvogen recalled Adalat CC starting Mar 7, 2017. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0635-2017 on Apr 12, 2017. Reason: Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib. Status: Terminated.

Why it was recalled

Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib

Product description

Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749601

Lot numbers, UPCs & expiration codes

Lot #: BXHD7U1A, Exp. 10/2018

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-0635-2017
Classification
Class III
Status
Terminated
Recall initiated
Mar 7, 2017
FDA report date
Apr 12, 2017
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
Alvogen, Inc

Original FDA data

Every field from FDA enforcement report D-0635-2017, exactly as published.

Show all FDA fields
City
Pine Brook
State
NJ
Status
Terminated
Country
United States
Event ID
76664
Address
10 Bloomfield Ave Bldg B Ste 2
Code information
Lot #: BXHD7U1A, Exp. 10/2018
Postal code
07058-9743
Report date
Apr 12, 2017
Product type
Drugs
Recall number
D-0635-2017
Classification
Class III
Recalling firm
Alvogen, Inc
Termination date
Dec 15, 2017
Reason for recall
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Voluntary / mandated
Voluntary: Firm initiated
Product description
Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749601
Distribution pattern
Nationwide
Recall initiation date
Mar 7, 2017
Initial firm notification
Letter
Center classification date
Apr 4, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0635-2017, published Apr 12, 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.

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