Docusate Calcium Softgel Capsules — Class II drug recall D-1451-2014
Terminated recall by Shamrock Medical Solutions Group LLC, reported 2014-07-30, distributed in CO, MA, OH, TX, WY. Labeling: Label Mix up; product labeled to contain Docusate Sodium 240mg instead of Docusate Calcium 240mg
| Recall number | D-1451-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Shamrock Medical Solutions Group LLC, Lewis Center, OH, United States |
| Recall initiated | 2011-09-27 |
| Classified | 2014-07-23 |
| Reported by FDA | 2014-07-30 |
| Terminated | 2014-07-31 |
| Distributed | CO, MA, OH, TX, WY |
| Quantity | 99 |
| Reason classes | labeling |
| NDC | 00904-5779-60 |
| Lot numbers | 002H79 |
| Expiration dates | 2013-06-19 |
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 for recall
Labeling: Label Mix up; product labeled to contain Docusate Sodium 240mg instead of Docusate Calcium 240mg
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1451-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.