RegWardenFDA facility compliance records
Recall

Class II — Ivoclar Vivadent, Inc.

Recalling firmIVOCLAR VIVADENT
Registered facilityView this company's 11 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusOngoing
ReasonAffected product may not perform as expected; the amalgam powder may not triturate correctly and the physical properties (i.e. strength, compression, working time, etc.) will be adversely affected.
ProductArticle No. NA6050411, Valiant PhD No. 1 Econo
Quantity2 boxes (500 per box)
DistributionUS Nationwide distribution in the states IN and TN.
Initiated2023-12-21
Classified2024-02-07
Recall numberZ-1006-2024
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 — Ivoclar Vivadent, Inc. (Z-1006-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93796/

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