Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

AHP NIFEdipine Capsules Recalled by Amerisource Health Services Due to Presence of Foreign Tablets/Capsules

Date: October 13, 2016
Company: Amerisource Health Services
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Amerisource Health Services directly.

Affected Products

AHP NIFEdipine Capsules, 10mg USP, 100 count carton (NDC: 68084-022-01); Individual Blister (NDC: 68084-022-11), Rx Only, Manufactured by: Actavis Elizabeth, LLC, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217

Quantity: 5283 cartons (100 capsules per carton = 528,300 capsules)

Why Was This Recalled?

Presence of Foreign Tablets/Capsules

Where Was This Sold?

US

About Amerisource Health Services

Amerisource Health Services has 23 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report