CLASS II Drug recall · Reported 22 Jan 2014 · FDA Enforcement Report

Benazepril HCL Tablet, 40 mg recalled by Aidapak Services

Aidapak Services is recalling Benazepril HCL Tablet, 40 mg, distributed in Arizona, California, Oregon, Washington. The recall was initiated on 2 Jul 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBENAZEPRIL HCL Tablet, 40 mg has the following codes Pedigree: AD49423_1, EXP: 5/16/2014; Pedigree: W003918, EXP: 6/28/2014; Pedigree: AD32757_7, EXP: 5/13/2014; Pedigree: AD68010_1, EXP: 5/28/2014.

Quantity recalled799 Tablets

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-713-2014
FDA event ID: 65707
Recalling firm: Aidapak Services, Vancouver, WA
Classification: Class II
Status: Terminated
Recall initiated: 2 Jul 2013
FDA classified: 16 Jan 2014
Reported: 22 Jan 2014
Type: Voluntary: Firm initiated
Customers notified by: Telephone
Reason category: Labeling Errors
Drug class: Blood Pressure Medication

Timeline

2 Jul 2013	Recall initiated by company
16 Jan 2014	Classified by FDA	+198 days
22 Jan 2014	Published 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

Labeling:Label Mixup; BENAZEPRIL HCL Tablet, 40 mg may be potentially mislabeled as NEFAZODONE HCL, Tablet, 200 mg, NDC 00093102506, Pedigree: AD46414_44, EXP: 5/16/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003931, EXP: 6/28/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD42592_1, EXP: 5/14/2014; ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/25

Product as listed by the FDA

BENAZEPRIL HCL Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162075410

Where it was distributed

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

Arizona California Oregon Washington

Questions about this recall

Is Benazepril HCL Tablet, 40 mg recalled?

Yes. Aidapak Services recalled Benazepril HCL Tablet, 40 mg on 2 Jul 2013. The recall is Class II and its status is Terminated. Recall number D-713-2014.

Why was it recalled?

Which lots are affected?

BENAZEPRIL HCL Tablet, 40 mg has the following codes Pedigree: AD49423_1, EXP: 5/16/2014; Pedigree: W003918, EXP: 6/28/2014; Pedigree: AD32757_7, EXP: 5/13/2014; Pedigree: AD68010_1, EXP: 5/28/2014.

Where was it sold?

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

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

More recalls from Aidapak Services

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29 Jan 2014Drug	CLASS II	Ascorbic Acid, Tablet, 500 mg, Over The Counter recalled	Aidapak Services	Labeling Errors	4 states
29 Jan 2014Drug	CLASS II	Calcitriol, Capsule, 25 mcg recalled by Aidapak Services	Aidapak Services	Packaging Defects	4 states

Other Benazepril recalls

All 3

Reported	Class	Recall	Company	Reason	Where
16 Oct 2019Drug	CLASS III	Benazepril HCl Tablets, USP 40 mg recalled by Amneal PharmaceuticalsBenazepril Hydrochloride	Amneal Pharmaceuticals	Other	Nationwide
22 Jan 2014Drug	CLASS II	Benazepril HCL Tablet, 5 mg recalled by Aidapak Services	Aidapak Services	Labeling Errors	4 states