PlainRecalls
FDA Devices Moderate Class II Terminated

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.

Reported: June 18, 2014 Initiated: April 14, 2014 #Z-1740-2014

Product Description

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.

Reason for Recall

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

Details

Recalling Firm
Ivoclar Vivadent, Inc.
Units Affected
241 units
Distribution
Worldwide Distribution: US Nationwide and the country of Canada.
Location
Buffalo, NY

Frequently Asked Questions

What product was recalled?
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.. Recalled by Ivoclar Vivadent, Inc.. Units affected: 241 units.
Why was this product recalled?
A stock check revealed broken glass fibers between the connector and the fiber bundle in a large number of these light probes.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 18, 2014. Severity: Moderate. Recall number: Z-1740-2014.