Actavis Laboratories, FL, Inc. recalls Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufac…

Recall date

March 26, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0488-2015

FDA classification

Class III

Brand / firm

Actavis Laboratories, FL, Inc.

Sold / distributed

Nationwide

Why it was recalled

Presence of Foreign Substance; fine residue or dust identified as aluminum may be on exterior of the capsule shell

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA --- NDC 62037-0600-90