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Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Complete recall history across all FDA and CPSC categories — 4 total recalls

Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (4)

FDA medical device enforcement actions by Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Date Product Reason Class
Feb 25, 2020 Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Tri... An issue within production process used to package trial kits let to the inc... Class II
Jul 13, 2018 Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution Immersion time stated on the bottle is 45 minutes while the product instructi... Class II
Sep 13, 2013 NX3 Try-In Gel. The product is used as a tooth shade resin material. Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because ... Class II
Feb 22, 2013 Kerr Maxcem Elite, self-etch/self-adhesive resin cement; Intro Kit Part No. 3... Kerr Corporation is initiating this recall because raw material used to prod... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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