Imodium Multi-Symptom Relief Caplets — Class III drug recall D-1404-2012
Terminated recall by Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc., reported 2012-07-11, distributed nationwide. Defective Container; damaged blister units
| Recall number | D-1404-2012 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc., Fort Washington, PA, United States |
| Recall initiated | 2012-05-17 |
| Classified | 2012-07-02 |
| Reported by FDA | 2012-07-11 |
| Terminated | 2013-04-11 |
| Distributed | Nationwide (US) |
| Quantity | 53,892 packages |
| Reason classes | packaging |
| Lot numbers | 07/13, CMF023 |
Product
Imodium Multi-Symptom Relief Caplets, Loperamide HCl 2 mg/Simethicone 125 mg, 18 count blister pack cartons, McNeil Consumer Healthcare, Div of McNeil-PPC Inc., Fort Washington, PA
Reason for recall
Defective Container; damaged blister units
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-1404-2012. 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.