PlainRecalls

Ivoclar Vivadent, Inc.

34 recalls on record · Latest: Feb 14, 2024

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Agency notice ledger

Federal filing book Ivoclar Vivadent, Inc. MID-BOOK · SINGLE-AGENCY

#495 of 14,151 · 34 notices · 0.033% archive

  • BOOK 34 notices
  • RANK #495 of 14,151
  • SHARE 0.033% archive
  • AGENCY FDA Devices (34)
  • CAT medical devices
  • CATS 1 category
  • LATEST Feb 14, 2024
  • PHOTO Colonia Care Pharmacy

Nearest notice-volume peer: Colonia Care Pharmacy (0 notice gap)

Ivoclar Vivadent, Inc. accounts for about 0.033% of the 104,423-notice archive on 34 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Ivoclar Vivadent, Inc. sits among 14,151 recalling firms

Ivoclar Vivadent, Inc. ranks 495th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Ivoclar Vivadent, Inc. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

34 495th of 14151 higher than 13,651 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Ivoclar Vivadent, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Ivoclar Vivadent, Inc. holds about 0.033% of archive notices alongside 34 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Feb 14, 2024

Article No. NA6050411, Valiant PhD No. 1 Econo

FDA Devices Low Feb 28, 2018

Heliomolar Refill 20x0.25g 110/A1, Product code 541501AN, Catalog number 541501

FDA Devices Low Feb 28, 2018

Heliomolar Refill 20x0.25g 140/A2, Product code 541502AN, Catalog number 541502

FDA Devices Low Feb 28, 2018

Heliomolar Refill 20x0.25g 110T, Product code 550559AN, Catalog number 550559

FDA Devices Low Feb 28, 2018

Heliomolar Refill 20x0.25g 210/A3, Product code 541503AN, Catalog number 541503

FDA Devices Moderate Dec 14, 2016

Virtual XD Test Pack Heavy/Light Fast Set, 2 x 50 ml, REF #/Product Code 646469, Rx ONLY -- Product Usage: Dental impression material

FDA Devices Moderate Dec 14, 2016

Virtual XD Refill Light Body Regular Set Wash Material, 2X50 ml, REF #/Product Code 646462, Rx ONLY -- Product Usage: Dental impression material

FDA Devices Moderate Dec 14, 2016

Virtual XD Refill Light Body Fast Set Wash Material, 2X50 ml, REF #/Product Code 646461, Rx ONLY -- product Usage: Dental impression material

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color A2 60ml, art. no. 681051. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color A1 60ml, art. no. 681050, Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color Impulse orange, art. no. 681168. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color D3 60ml, art. no. 681064. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color C2 60ml art. no. 681060. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color A3.5 60ml, art. no. 681053. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color Impulse violet, art. no. 681166 Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color D4 60ml, art. no. 681065. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color Impulse blue, Art. no. 681165 Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color Impulse grey, art. no. 681167 Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color B3 60ml, art. no. 681057. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color A4 60ml, art. no. 681054. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color Impulse brown, art. no. 681169 Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color B1 60ml, art. no. 681055. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color C4 60ml, art. no. 681062. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color D2 60ml, art. no. 681063. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color B4 60ml, art. no. 681058. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color B2 60ml, art. no. 681056. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color C1 60ml, art. no. 681059. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color A3 60ml, art. no. 681052. Product Usage: For coloring dental porcelain

FDA Devices Moderate Oct 12, 2016

Zenostar MT Color C3 60ml, art. no. 681061. Product Usage: For coloring dental porcelain

FDA Devices Moderate Aug 17, 2016

OptraPol Polishing Discs, Rx ONLY: OptraPol Refill Cup /10: REF/Product ID 634459, OptraPol Refill Small Flame/10: REF/Product ID 634458, OptraPol Assortment: REF/Product ID 634464 --Device Listing # B106952. One step polishing system for all common dental composites and amalgam.

FDA Devices Moderate Mar 9, 2016

Helioseal Clear Refill 1 x 1.25 g, REF/Product Code/Art. No. 558521AN and Helioseal Clear Assortment 5 x 1.25 g, REF/Product Code/Art. No. 558520AN ---- COMMON/USUAL NAME: Pit & Fissure Sealant

FDA Devices Moderate Aug 5, 2015

IPS Empress Universal Glaze Spray 270 mL, Product Code/Model/Catalog Number 609432AN, Rx only. Porcelain glaze spray used in the fabrication of dental restorations

FDA Devices Moderate Jun 18, 2014

bluephase style Light probe Pin-point 6>2 mm black REF # 636 241. The accessory is a pin point light probe, an accessory to a dental curing light Ultraviolet activator for polymerization for use during dental curing.

FDA Devices Moderate Nov 27, 2013

ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations

Ivoclar Vivadent, Inc. holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (34 here — heavy-book).

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Frequently Asked Questions

How many federal recall notices name Ivoclar Vivadent, Inc.?
PlainRecalls indexes 34 distinct federal recall events naming Ivoclar Vivadent, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Ivoclar Vivadent, Inc. sit among other recalling firms?
Ivoclar Vivadent, Inc. ranks #495 of 14,151 by distinct recall-event count among 14,151 firms in this archive (96th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Ivoclar Vivadent, Inc.'s notices?
FDA Devices accounts for 34 of this firm's 34 indexed notices.
What product category dominates Ivoclar Vivadent, Inc.'s filing book?
Filings for Ivoclar Vivadent, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous?
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Ivoclar Vivadent, Inc.: 34 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Ivoclar Vivadent, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026