CLASS II Drug recall · Reported 21 Aug 2019 · FDA Enforcement Report

Macrobid Urinary Tract Anitbacterial, 100 mg recalled by Alvogen

Alvogen is recalling Macrobid Urinary Tract Anitbacterial, 100 mg, distributed in Puerto Rico. The recall was initiated on 24 Jul 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 472990, Exp 03/2020
NDC52427-285
UPC0352427285011
Quantity recalled4272 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1723-2019
FDA event ID
83434
Recalling firm
Alvogen, Pine Brook, NJ
Manufacturer
Almatica Pharma LLC
Classification
Class II
Status
Terminated
Recall initiated
24 Jul 2019
FDA classified
12 Aug 2019
Reported
21 Aug 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay
Drug class
Antibiotics

Timeline

24 Jul 2019Recall initiated by company
12 Aug 2019Classified by FDA+19 days
21 Aug 2019Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Failed dissolution specifications

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

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

Where it was distributed

Natonwide, PR

Puerto Rico

Questions about this recall

Why was it recalled?

Failed dissolution specifications

Which lots are affected?

Lot # 472990, Exp 03/2020

Where was it sold?

Natonwide, PR

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 83434
ReportedClassRecallCompanyReasonWhere
CLASS IINitrofurantoin Monohydrate/Macrycrystals Capsules, 100 mg recalledNitrofurantoin Monohydrate/ MacrocrystallineAlvogenPotency & AssayPR

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