Kerr Corporation

Complete recall history across all FDA and CPSC categories — 5 total recalls

Kerr Corporation 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 (5)

FDA medical device enforcement actions by Kerr Corporation

Date Product Reason Class
May 29, 2014 Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3... Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number ... Class II
Oct 25, 2012 BioPlant, a dental bone grafting material. BioPlant has been assigned the pr... The firm initiated the recall becaue disturbing the BioPlant product soon aft... Class II
Apr 10, 2012 The brand name of the device is Laser Loupes, a dentalloupe with laser eye ... The firm initiated the recall for Laser Loupes because the ink used to mark w... Class II
Feb 21, 2012 The brand name of the device is AlgiNot, a dental impression material. Produ... The firm recalled the product because it may cure harder than expected within... Class II
Nov 17, 2011 Freedom Cordless LED Light System. Freedom System, Standard Length, Part Numb... The firm recalled the Freedom Cordless LED Headlight because some units were ... 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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