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

Multivitamin/Multimineral Tablet recalled by Aidapak Services

Aidapak Services is recalling Multivitamin/Multimineral Tablet, 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 codesMULTIVITAMIN/MULTIMINERAL Tablet has the following codes Pedigree: AD62979_1, EXP: 5/23/2014; Pedigree: W003553, EXP: 6/24/2014.

Quantity recalled1,000 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-710-2014
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: Vitamins & OTC Supplements

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; MULTIVITAMIN/MULTIMINERAL Tablet may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: AD62865_13, EXP: 5/23/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003514, EXP: 6/21/2014.

Product as listed by the FDA

MULTIVITAMIN/MULTIMINERAL Tablet, Distributed by: AidaPak Service, LLC, NDC 65162066850

Where it was distributed

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

Arizona California Oregon Washington

Questions about this recall

Is Multivitamin/Multimineral Tablet recalled?

Yes. Aidapak Services recalled Multivitamin/Multimineral Tablet on 2 Jul 2013. The recall is Class II and its status is Terminated. Recall number D-710-2014.

Why was it recalled?

Which lots are affected?

MULTIVITAMIN/MULTIMINERAL Tablet has the following codes Pedigree: AD62979_1, EXP: 5/23/2014; Pedigree: W003553, EXP: 6/24/2014.

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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Reported	Class	Recall	Company	Reason	Where
29 Jan 2014Drug	CLASS II	MERCapsuleTOPURINE, Tablet, 50 mg recalled by Aidapak Services	Aidapak Services	Labeling Errors	4 states
29 Jan 2014Drug	CLASS II	Selenium, Tablet, 50 mcg, Over The Counter recalled by Aidapak Services	Aidapak Services	Labeling Errors	4 states
29 Jan 2014Drug	CLASS II	Venlafaxine HCL, Tablet, 100 mg recalled by Aidapak Services	Aidapak Services	Labeling Errors	4 states
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 Multivitamin/multimineral recalls

All 3

Reported	Class	Recall	Company	Reason	Where
22 Jan 2014Drug	CLASS II	Multivitamin/Multimineral Tablet recalled by Aidapak Services	Aidapak Services	Labeling Errors	4 states
22 Jan 2014Drug	CLASS II	Multivitamin/Multimineral Tablet, Over The Counter recalled	Aidapak Services	Labeling Errors	4 states