CLASS II Drug recall · Reported 25 Jan 2023 · FDA Enforcement Report

Rifampin Capsules USP, 300 mg (10 recalled

Amerisource Health Services is recalling Rifampin Capsules USP, 300 mg (10 x per, distributed nationwide in the US. The recall was initiated on 20 Dec 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 1007805, exp. 12/31/2023
Quantity recalled3,091 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-0165-2023
FDA event ID
91416
Recalling firm
Amerisource Health Services, Columbus, OH
Classification
Class II
Status
Terminated
Recall initiated
20 Dec 2022
FDA classified
18 Jan 2023
Reported
25 Jan 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

20 Dec 2022Recall initiated by company
18 Jan 2023Classified by FDA+29 days
25 Jan 2023Published 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 Impurities/Degradations Specifications

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

Rifampin Capsules USP, 300 mg, 100 Capsules (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 60687-586-01 (Individual Dose NDC: 60687-586-11)

Where it was distributed

Nationwide in the USA.

Nationwide

Questions about this recall

Why was it recalled?

Failed Impurities/Degradations Specifications

Which lots are affected?

Lot #: 1007805, exp. 12/31/2023

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 1 Oct 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 Amerisource Health Services

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