Reported Feb 28, 2018 · Terminated

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

Ivoclar Vivadent, Inc.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Ivoclar Vivadent, Inc. · 175 Pineview Dr · Amherst, NY · 14228-2231

Is this the product you have?

    • Heliomolar Refill 20x0.25g 210/A3
    • Product code 541503AN
    • Catalog number 541503
Lot codes and dates
  • BatchV37905, Exp
  • date21.10.2020
  • BatchV45006, Exp
  • date04.12.2020
  • BatchV49583, Exp
  • date12.01.2021
  • BatchW04412, Exp
  • date20.02.2021
  • BatchW13322, Exp
  • date07.04.2021
Amount recalled
1,244 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Why it was recalled

Complaints were filed claiming the material consistency was too soft and too sticky in comparison to its usual consistency, causing unexpected handling for the user during packing and contouring.

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 28, 2018 · Data as of Sep 19, 5:29 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.