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

Zinc Sulfate Capsule, 220 mg, Over The Counter recalled

Aidapak Services is recalling Zinc Sulfate Capsule, 220 mg, Over The Counter, 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 codesZINC SULFATE, Capsule, 220 mg has the following codes Pedigree: AD52993_34, EXP: 5/20/2014; Pedigree: W003641, EXP: 6/25/2014.

Quantity recalled200 Capsules

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-651-2014
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

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; ZINC SULFATE Capsule, 220 mg may be potentially mislabeled as CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD52778_10, EXP: 5/20/2014; CALCITRIOL, Capsule, 0.25 mcg, NDC 00054000725, Pedigree: W003638, EXP: 6/25/2014.

Product as listed by the FDA

ZINC SULFATE Capsule, 220 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258013101

Where it was distributed

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

Arizona California Oregon Washington

Questions about this recall

Is Zinc Sulfate Capsule, 220 mg, Over The Counter recalled?

Yes. Aidapak Services recalled Zinc Sulfate Capsule, 220 mg, Over The Counter on 2 Jul 2013. The recall is Class II and its status is Terminated. Recall number D-651-2014.

Why was it recalled?

Which lots are affected?

ZINC SULFATE, Capsule, 220 mg has the following codes Pedigree: AD52993_34, EXP: 5/20/2014; Pedigree: W003641, EXP: 6/25/2014.

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.

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15 Oct 2025Drug	CLASS II	Zinc Sulfate for Injection, all strengths and presentations recalled	GenoGenix	Sterility	Nationwide
22 May 2013Drug	CLASS II	Zinc Sulfate Injection, all strengths recalled by FVS Holdings	FVS Holdings	Sterility	Nationwide