Kerr Corp OptiBond Solo Plus Self-Etch Adhesive System, Part Number 31966 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OptiBond Solo Plus Self-Etch Adhesive System, Part Number 31966
Brand
Kerr Corp
Lot Codes / Batch Numbers
Lot numbers: 448798, 449556 and 451706
Products Sold
Lot numbers: 448798, 449556 and 451706
Kerr Corp is recalling OptiBond Solo Plus Self-Etch Adhesive System, Part Number 31966 due to Mis-pack/mis-label: The OptiBond Self Etch Primer and OptiBond Solo Plus Adhesive in the chambers were mis-packaged/mis-labeled in reverse order. Appl. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mis-pack/mis-label: The OptiBond Self Etch Primer and OptiBond Solo Plus Adhesive in the chambers were mis-packaged/mis-labeled in reverse order. Application of these products in reverse order may result in compromised bond strength.
Recommended Action
Per FDA guidance
A total of thirty-four (34) consignees were sent the recall communication via USPS 1st class mail on August 29, 2006. There will be an additional five (5) letters that will be sent to consignees in Europe once the recall communication is translated into their respective languages. The consignees were instructed to complete the Return Form and return any affected product in their inventory. They were also requested to recover any affected product that they may have shipped to their customers. Periodic effectiveness checks will be conducted in order to follow up with non-responders.
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