Kerr Corporation: Medical Device Recall in 2014 - (Recall #: Z-1788-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: May 29, 2014

Date Posted: June 25, 2014

Recall Number: Z-1788-2014

Event ID: 68426

Reason for Recall:

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.

Status: Terminated

Product Quantity: 2,030 units

Code Information:

Part Number 29948, Lot Number 3-1294. Expires October 2016

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated