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Ivoclar Vivadent, Inc. recalls bluephase style Light probe Pin-point 6>2 mm black REF # 636 241. The accessory is a pin point light probe, an accessor
Recalled June 18, 2014 · FDA recall Z-1740-2014 · Ivoclar Vivadent
Hazard
A stock check revealed broken glass fibers between the connector and the fiber bundle in a large number of these light probes. · FDA Class II
Units
241 units
Sold at
Worldwide Distribution: US Nationwide and the country of Canada.
Description
A stock check revealed broken glass fibers between the connector and the fiber bundle in a large number of these light probes.
Product
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.
Manufacturer(s)
Ivoclar Vivadent, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →