CLASS III Drug recall · Reported 1 Nov 2017 · FDA Enforcement Report

Enalapril Maleate Tablets, USP, 5MG recalled by Aidarex Pharmaceuticals

Aidarex Pharmaceuticals is recalling Enalapril Maleate Tablets, USP, 5MG, distributed in Florida. The recall was initiated on 5 Sep 2017 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot #: 55097-2, 56085-1, Exp 11/30/2018
Quantity recalled12 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-0053-2018
FDA event ID
78106
Recalling firm
Aidarex Pharmaceuticals, Corona, CA
Classification
Class III
Status
Terminated
Recall initiated
5 Sep 2017
FDA classified
26 Oct 2017
Reported
1 Nov 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Potency & Assay

Timeline

5 Sep 2017Recall initiated by company
26 Oct 2017Classified by FDA+51 days
1 Nov 2017Published in enforcement report+6 days

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

Reason for recall

Failed Impurities/Degradation Specifications: manufacturer of product recalled this repackaged lot due to out of specification results for related compound.

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

ENALAPRIL MALEATE Tablets, USP, 5MG, 90-count bottles, Rx only, MFG: Wockhardt Ltd., India; Packaged By: Aidarex Pharmaceuticals; NDC 33261-0693-90.

Where it was distributed

Product was distributed in Florida

Florida

Questions about this recall

Why was it recalled?

Failed Impurities/Degradation Specifications: manufacturer of product recalled this repackaged lot due to out of specification results for related compound.

Which lots are affected?

Lot #: 55097-2, 56085-1, Exp 11/30/2018

Where was it sold?

Product was distributed in Florida

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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.

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