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All product recalls associated with Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical.
Total Recalls
51
Past Year
0
Class I (Serious)
0
Most Recent
Feb 2020
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
An issue within production process used to package trial kits let to the inclusion of the incorrect bonding agent for the kit. Use of the incorrect bonding agent may lead to increased risk of bond failures.
The recall was initiated because the catalyst portion of the syringe may have polymerized, therefore making the product unusable.
Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.