CLASS II Drug recall · Reported 26 Jun 2019 · FDA Enforcement Report

Anastrozole Tablets, USP, 1mg unit dose blisters recalled

American Health Packaging is recalling Anastrozole Tablets, USP, 1mg unit dose blisters per, distributed nationwide in the US. The recall was initiated on 9 May 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 175289A, 175286B, 175290B, Exp. 08/31/2019; 179906A, Exp. 03/31/2020; 183252A, Exp. 09/30/2020; 184611A, Exp. 11/30/2020
NDC60687-112
Quantity recalled15,386 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-1394-2019
FDA event ID
82854
Recalling firm
American Health Packaging, Columbus, OH
Manufacturer
American Health Packaging
Classification
Class II
Status
Terminated
Recall initiated
9 May 2019
FDA classified
19 Jun 2019
Reported
26 Jun 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Processing Deviation

Timeline

9 May 2019Recall initiated by company
19 Jun 2019Classified by FDA+41 days
26 Jun 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

GMP Deviations: Potential cross contamination due to cleaning procedure failure.

The USDA issues these when meat or poultry was produced without proper inspection, or when a step such as cooking or pasteurisation did not meet requirements.

Product as listed by the FDA

Anastrozole Tablets, USP, 1mg, 30-count unit dose blisters per carton, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC 60687-112-21.

Where it was distributed

Nationwide within the USA

Nationwide

Questions about this recall

Why was it recalled?

GMP Deviations: Potential cross contamination due to cleaning procedure failure.

Which lots are affected?

Lot #: 175289A, 175286B, 175290B, Exp. 08/31/2019; 179906A, Exp. 03/31/2020; 183252A, Exp. 09/30/2020; 184611A, Exp. 11/30/2020

Where was it sold?

Nationwide within 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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