US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 27, 2011 (15 years ago)

Docusate Calcium Softgel Capsules, 240 mg, OTC, packaged and labeled to contain Docusate…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Labeling: Label Mix up; product labeled to contain Docusate Sodium 240mg instead of Docusate Calcium 240mg

What was recalled

Docusate Calcium Softgel Capsules, 240 mg, OTC, packaged and labeled to contain Docusate Sodium 240mg, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Major Pharmaceuticals, Livonia, MI NDC 00904-5779-60

Recalling firm
Shamrock Medical Solutions Group LLC
NDC code
00904-5779-60
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1451-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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