Kerr Corp 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
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Kerr Corp
Lot Codes / Batch Numbers
Part Number 33351, Lot Numbers: 3252902, 3229807, 3268505, 3277455, 3257280, 3258772 and 3269811.
Products Sold
Part Number 33351, Lot Numbers: 3252902, 3229807, 3268505, 3277455, 3257280, 3258772 and 3269811.
Kerr Corp is recalling Kerr TempBond Clear, Part # 33351, 1717 West Collins Avenue, Orange, CA 92867. Intended for use in due to The recall was initiated because the catalyst portion of the syringe may have polymerized, therefore making the product unusable.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The recall was initiated because the catalyst portion of the syringe may have polymerized, therefore making the product unusable.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026