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Class II: temporary or reversible health riskTerminated

Alvogen Macrobid Urinary Tract Anitbacterial Recall

Macrobid Urinary Tract Anitbacterial, 100 mg, 100-count bottle, Rx Only, Mfg

Alvogen, Inc · Pine Brook, NJ

Risk level
Class II
Reported by FDA
Aug 21, 2019
Recall ID
D-1723-2019
Check your lot numberHow we source this data

Summary

Alvogen recalled Macrobid Urinary Tract Anitbacterial starting Jul 24, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1723-2019 on Aug 21, 2019. Reason: Failed dissolution specifications. Status: Terminated.

Why it was recalled

Failed dissolution specifications

Product description

Macrobid Urinary Tract Anitbacterial, 100 mg, 100-count bottle, Rx Only, Mfg. by: Norwich Pharmaceuticals, Inc. Norwich, NY 13815 USA Dist. by: Almatica Pharma, Inc. Pine Brook, NJ 07058 USA, NDC 52427-285-01

Lot numbers, UPCs & expiration codes

Lot # 472990, Exp 03/2020

Where it was sold

Natonwide, PR

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-1723-2019
Classification
Class II
Status
Terminated
Recall initiated
Jul 24, 2019
FDA report date
Aug 21, 2019
Quantity
4272 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Alvogen, Inc

Original FDA data

Every field from FDA enforcement report D-1723-2019, exactly as published.

Show all FDA fields
City
Pine Brook
State
NJ
Status
Terminated
Country
United States
Event ID
83434
Address
10 Bloomfield Ave Bldg B Ste 2
Code information
Lot # 472990, Exp 03/2020
Postal code
07058-9743
Report date
Aug 21, 2019
Product type
Drugs
Recall number
D-1723-2019
Classification
Class II
Recalling firm
Alvogen, Inc
Product quantity
4272 bottles
Termination date
Aug 4, 2021
Reason for recall
Failed dissolution specifications
Voluntary / mandated
Voluntary: Firm initiated
Product description
Macrobid Urinary Tract Anitbacterial, 100 mg, 100-count bottle, Rx Only, Mfg. by: Norwich Pharmaceuticals, Inc. Norwich, NY 13815 USA Dist. by: Almatica Pharma, Inc. Pine Brook, NJ 07058 USA, NDC 52427-285-01
Distribution pattern
Natonwide, PR
Recall initiation date
Jul 24, 2019
Initial firm notification
Letter
Center classification date
Aug 12, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1723-2019, published Aug 21, 2019. 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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