FDA Recall Terminated

Kerr TempBond Clear, Part # 33351, 1717 West Collins Avenue, Orange, CA 92867. Intended for use in a dual-cured, temporary resin-based cement designed to be used in conjunction with temporary restoration such as crowns, bridges, inlays and onlays.

Recall: Z-0074-2010 · Initiated September 9, 2009

Recall

Recall Number
Z-0074-2010
Event Number
53296
Firm
Kerr Corp
FEI Number
2024312
Product Code
EMA
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
September 9, 2009
Posted
October 23, 2009
Terminated
December 12, 2011
Address
1717 W Collins Ave, Orange, CA, 92867

Description

Kerr TempBond Clear, Part # 33351, 1717 West Collins Avenue, Orange, CA 92867. Intended for use in a dual-cured, temporary resin-based cement designed to be used in conjunction with temporary restoration such as crowns, bridges, inlays and onlays.

Reason

The recall was initiated because the catalyst portion of the syringe may have polymerized, therefore making the product unusable.

Action

Kerr Corporation issued an "Urgent Medical Device Recall" dated September 8, 2009. The letter informed customers that the product recalled was shipped to their establishment between June and July 2009 and if they have any of the affected products listed to contact Kerr Customer Care at 1-800-537-7123 to receive an RMA number. The RMA will allow for a quick return and replacement or credit.

Distribution

Worldwide Distribution -- United States, Canada, Mexico, Hong Kong, Israel, Singapore, Colombia, Dominican Republic and Europe.

Quantity

13,518 units