REUMOFAN PLUS Tablets — Class I drug recall D-1322-2014
Terminated recall by Pain Free By Nature, reported 2014-05-21, distributed nationwide. Marketed Without an Approved NDA/ANDA; Product contains undeclared diclofenac and methocarbamol.
| Recall number | D-1322-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pain Free By Nature, Harper, KS, United States |
| Recall initiated | 2014-03-13 |
| Classified | 2014-05-15 |
| Reported by FDA | 2014-05-21 |
| Terminated | 2015-06-01 |
| Distributed | Nationwide (US) |
| Quantity | 7,123 bottles |
| Reason classes | undeclared allergen, unapproved product |
Product
REUMOFAN PLUS Tablets, 30 Tablet Bottles, OTC. Previene el cancer en los huesos, Nueva presentacion el original.
Reason for recall
Marketed Without an Approved NDA/ANDA; Product contains undeclared diclofenac and methocarbamol.
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-1322-2014. 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.