CLASS II Drug recall · Reported 7 Aug 2019 · FDA Enforcement Report

Doxycycline Hyclate Tablets, USP, 100 mg per carton recalled

American Health Packaging is recalling Doxycycline Hyclate Tablets, USP, 100 mg per carton ( Unit Dose Blisters), distributed nationwide in the US. The recall was initiated on 1 Aug 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 172569, Exp 7/31/2019
NDC62584-693
Quantity recalled6,579 cartons

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-1582-2019
FDA event ID
83466
Recalling firm
American Health Packaging, Columbus, OH
Manufacturer
American Health Packaging
Classification
Class II
Status
Terminated
Recall initiated
1 Aug 2018
FDA classified
31 Jul 2019
Reported
7 Aug 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay
Drug class
Antibiotics

Timeline

1 Aug 2018Recall initiated by company
31 Jul 2019Classified by FDA+364 days
7 Aug 2019Published in enforcement report+7 days

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

Reason for recall

Failed Dissolution Specifications: Out of specification result for the dissolution test.

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

Doxycycline Hyclate Tablets, USP, 100 mg, 30 Tablets per carton (3 x 10 Unit Dose Blisters), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio, 43217, NDC Carton: 62584-693-21; NDC Unit Dose: 62584-693-11

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Failed Dissolution Specifications: Out of specification result for the dissolution test.

Which lots are affected?

Lot 172569, Exp 7/31/2019

Where was it sold?

Nationwide in the USA

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 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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