RegWardenFDA facility compliance records
Recall

Class II — Ultradent Products, Inc.

Recalling firmULTRADENT PRODUCTS, INC.
Registered facilityUltradent Products Inc. (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonComposite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
ProductJiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.
Quantity2508
DistributionUS: MA, WI, ME, AL, NY, MN, CA, KY, IL, WY, WA, OH, PR, CT, OR, NJ, MI, NC, HI, PA, NE, TX, UT, NV, LA, VA, MO, FL, AZ, WV, IA.
Initiated2026-01-28
Classified2026-03-27
Recall numberZ-1689-2026
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 — Ultradent Products, Inc. (Z-1689-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98419/

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