RecallRadar

FDA Drug recall D-1451-2014

Docusate Calcium Softgel Capsules, 240 mg, OTC, packaged and labeled to contain Docusate Sodium 240mg, Repackaged By: Shamrock Medical Solu…

On 2014-07-30 the FDA classified a Class II recall of Docusate Calcium Softgel Capsules, 240 mg, OTC, packaged and labeled to contain Docusate Sodium 240mg, Repackaged By: Shamrock Medical Solu… by Shamrock Medical Solutions Group, citing labeling: Label Mix up; product labeled to contain Docusate Sodium 240mg instead of Docusate Calcium 240mg.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1451-2014
ClassificationClass II
Statusterminated
Initiated2011-09-27
Published2014-07-30
Last updated2026-09-13 11:51 UTC
CompanyShamrock Medical Solutions Group
DistributionCO, MA, OH, TX, WY

Product

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

Reason

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

Identifiers

code_infoLot #: 002H79, Use By: 06/19/2013, NDC: 00904-5779-60

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1451-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.