CLASS II Drug recall · Reported 5 Jul 2017 · FDA Enforcement Report

Doxycycline Hyclate USP, active pharmaceutical ingredient, a) recalled

American Pharmaceutical Ingredients is recalling Doxycycline Hyclate USP, active pharmaceutical ingredient, a), distributed nationwide in the US. The recall was initiated on 1 Jun 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 082815-1, EXP 06/04/2019
Quantity recalled23.5kg

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-0927-2017
FDA event ID
77525
Recalling firm
American Pharmaceutical Ingredients, Waterford, MI
Classification
Class II
Status
Terminated
Recall initiated
1 Jun 2017
FDA classified
29 Jun 2017
Reported
5 Jul 2017
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Labeling Errors
Drug class
Antibiotics

Timeline

1 Jun 2017Recall initiated by company
29 Jun 2017Classified by FDA+28 days
5 Jul 2017Published 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: Not Elsewhere Classified. Manufacturer and product were discovered to be on FDA Import Alert 66-66 for misbranding of active pharmaceutical ingredient.

Product as listed by the FDA

Doxycycline Hyclate USP, active pharmaceutical ingredient, a) 25 g packaged in a 500 cc container (NDC: 58597-8082-4), b) 100 g packaged in 16 oz container (NDC: 58597-8082-6), c) 500 g packaged in a 2500 cc container (NDC: 58597-8082-7) and a 1,000 g packaged in 1 gallon container (NDC: 58597-8082-8). For Prescription Compounding RX Only. Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

Where it was distributed

Nationwide in the US

Nationwide

Questions about this recall

Why was it recalled?

Labeling: Not Elsewhere Classified. Manufacturer and product were discovered to be on FDA Import Alert 66-66 for misbranding of active pharmaceutical ingredient.

Which lots are affected?

Lot: 082815-1, EXP 06/04/2019

Where was it sold?

Nationwide in the US

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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