Reported Jun 18, 2014 · Terminated

bluephase style Light probe Pin-point 6>2 mm black REF # 636 241. The accessory is a pin point light probe, an…

Ivoclar Vivadent, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

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 · Buffalo, NY · 14228-2231

Is this the product you have?

  • 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.
Lot codes and dates
  • Reference number 636241, all lots
Amount recalled
241 units

Where it was sold

  • Nationwide

Why it was recalled

A stock check revealed broken glass fibers between the connector and the fiber bundle in a large number of these light probes.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 5, 2015 · Data as of Sep 19, 6:12 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.