RecallWatchUSA

Home / Recalls / Medical Devices

Kerr Corporation recalls Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The intended use of this device i

Recalled June 25, 2014 · FDA recall Z-1788-2014 · Kerr

Hazard
Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number 29948, Lot Number 3-1294), because it may set faster than specified in the Directions for Use. · FDA Class II
Units
2,030 units
Sold at
Worldwide Distribution-USA (nationwide) and the countries of Canada, Mexico, Australia, Belgium, Czech Republic, Germany, Spain, France, Great Britain, French Guiana, Italy, Portugal, and Saudi Arabia.

Description

Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number 29948, Lot Number 3-1294), because it may set faster than specified in the Directions for Use.

Product
Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The intended use of this device is to be used as a dental restorative material in the treatment of dental caries.
Manufacturer(s)
Kerr Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Kerr Corporation recalls Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The intended use of this device i | RecallWatchUSA