Overview of recall records associated with Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical, including dates, categories and classifications where available.
Classification mix: Class II: 2.
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…
Immersion time stated on the bottle is 45 minutes while the product instructions say 90 minutes.
This page summarizes recall records in which the official source identifies Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
