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Recall

Class II — Dharma Research, Inc.

Recalling firmDharma Research, Inc.
Registered facilityDharma Research/Medeco International (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonDuring an FDA inspection, it was found that the products are being marketed without a cleared 510k.
ProductDharma Cavity Varnish with Fluoride
Quantity2,842
DistributionWorldwide Distribution: US Distribution in states of: CA, PA, FL, IL, including Puerto Rico; and countries of: Honduras, Dominican Republic, Turkey, Nicaragua, Colombia, Pakistan, Trinidad & Tobago, Guatemala, Phillipines, Saudi Arabia, and United Arab Emirates.
Initiated2014-09-29
Classified2014-11-26
Terminated2016-10-03
Recall numberZ-0475-2015
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Dharma Research, Inc. (Z-0475-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69386/

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