Class III โ€” Low Risk

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

Candesartan Cilexetil Tablets Recalled by Amerisource Health Services Due to Failed Impurities/Degradation Specifications; 9 month stability (manufacturer)

Date: January 26, 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

Candesartan Cilexetil Tablets, 16 mg, 30 Tablets (5 x 6) blister pack, Rx, Distributed by: American Health Packaging Columbus, Ohio 43217, NDC 68084-877-25(carton), NDC 68084-877-95(individual dose)

Quantity: 716 cartons

Why Was This Recalled?

Failed Impurities/Degradation Specifications; 9 month stability (manufacturer)

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Amerisource Health Services

Amerisource Health Services has 23 total recalls tracked by RecallDetector.

Related Recalls

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