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

Quinapril HCL Tablet, 10 mg recalled by Aidapak Services

Aidapak Services is recalling Quinapril HCL Tablet, 10 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 codesQUINAPRIL HCL, Tablet, 10 mg has the following code Pedigree: AD42611_4, EXP: 5/14/2014.

Quantity recalled90 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-650-2014
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; QUINAPRIL HCL Tablet, 10 mg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 80 mg, NDC 23155011401, Pedigree: AD42566_4, EXP: 5/14/2014.

Product as listed by the FDA

QUINAPRIL HCL Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762502001

Where it was distributed

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

Arizona California Oregon Washington

Questions about this recall

Is Quinapril HCL Tablet, 10 mg recalled?

Yes. Aidapak Services recalled Quinapril HCL Tablet, 10 mg on 2 Jul 2013. The recall is Class II and its status is Terminated. Recall number D-650-2014.

Why was it recalled?

Labeling:Label Mixup; QUINAPRIL HCL Tablet, 10 mg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 80 mg, NDC 23155011401, Pedigree: AD42566_4, EXP: 5/14/2014.

Which lots are affected?

QUINAPRIL HCL, Tablet, 10 mg has the following code Pedigree: AD42611_4, EXP: 5/14/2014.

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
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Other Quinapril recalls

All 9

Reported	Class	Recall	Company	Reason	Where
28 Dec 2022Drug	CLASS II	Quinapril Tablets USP, 40 mg recalled by Lupin PharmaceuticalsQuinapril	Lupin Pharmaceuticals	Nitrosamine Impurity	Nationwide
28 Dec 2022Drug	CLASS II	Quinapril Tablets USP, 20 mg recalled by Lupin PharmaceuticalsQuinapril	Lupin Pharmaceuticals	Nitrosamine Impurity	Nationwide
12 Apr 2017Drug	CLASS III	Quinapril Tablets USP 5 mg, Lupin Pharmaceuticals, Inc. recalledQuinapril	Lupin Pharmaceuticals	Potency & Assay	Nationwide
11 Mar 2015Drug	CLASS III	Quinapril Tablets USP, 5 mg recalled by AVKARE	AVKARE	Potency & Assay	Nationwide
11 Mar 2015Drug	CLASS III	Quinapril Tablets USP, 40 mg recalled by AVKARE	AVKARE	Potency & Assay	Nationwide