Severity
Critical
FDA Drug recall · Reported May 21, 2014
Marketed Without an Approved NDA/ANDA; Product contains undeclared diclofenac and methocarbamol.
Pain Free By Nature recalled REUMOFAN PLUS Tablets, 30 Tablet Bottles, OTC. Previene el cancer en los huesos, Nueva p… - a critical-severity action.
REUMOFAN PLUS Tablets, 30 Tablet Bottles, OTC. Previene el cancer en los huesos, Nueva p… was recalled by Pain Free By Nature in May 21, 2014. Reason: Marketed Without an Approved NDA/ANDA; Product contains undeclared diclofenac and methocarbamol.. Check the official notice for the remedy. Verify recall #D-1322-2014 with the FDA Drug before acting.
The recall
Pain Free By Nature issued this critical-severity FDA Drug recall-Marketed Without an Approved NDA/ANDA; Product contains undeclared diclofenac and methocarbamol..
Sourced from official FDA Drug enforcement records. Verify recall #D-1322-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-1322-2014) was formally reported on May 21, 2014, with the manufacturer initiating the action on March 13, 2014. It is classified under Critical severity (Class I), with a current status of Terminated. Pain Free By Nature is listed as the recalling firm, operating out of Harper, KS. Federal records list the affected scope as 7,123 bottles.
The documented reason for this recall is: Marketed Without an Approved NDA/ANDA; Product contains undeclared diclofenac and methocarbamol. Distribution data in the federal record shows the product reached: Nationwide including Puerto Rico. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Critical
Affected scope
7,123 bottles
Related Recalls
6
5 from same agency
REUMOFAN PLUS Tablets, 30 Tablet Bottles, OTC. Previene el cancer en los huesos, Nueva presentacion el original.
Marketed Without an Approved NDA/ANDA; Product contains undeclared diclofenac and methocarbamol.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-1322-2014 |
| Date reported | May 21, 2014 |
| Date initiated | March 13, 2014 |
| Recalling firm | Pain Free By Nature |
| Firm location | Harper, KS |
| Affected scope | 7,123 bottles |
| Distribution | Nationwide including Puerto Rico |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Lupin Pharmaceuticals Inc. · 2026-05-27
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported May 21, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.