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Threshold Enterprises Ltd

Complete recall history across all FDA and CPSC categories — 8 total recalls

Threshold Enterprises Ltd 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.

Food Recalls (8)

FDA food safety enforcement actions by Threshold Enterprises Ltd

Date Product Reason Class
Sep 10, 2019 Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Suppor... Labeling error; incorrect supplement facts panel and label claims for two ing... Class III
Dec 7, 2018 Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF000... Recall of Mullein Lung Complex due to a labeling error which indicates the i... Class II
Jun 16, 2017 Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and... Product was inadvertently released prior to release of all QC testing. Testin... Class II
Dec 12, 2016 Source Naturals Dietary Supplement Vitamin D-3; Bioactive Form for Bone an... Testing of Vitamin D-3 as a result of a consumer complaint found specific lot... Class II
Sep 11, 2015 Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, ... Dietary supplements contain low levels of undeclared boron Class II
Sep 11, 2015 Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; ... Dietary supplements contain low levels of undeclared boron Class II
Nov 22, 2013 Source Naturals Essential Enzyme Ultra VEGI-CAP: Premium Digestive Enzyme Bl... Dietary Supplements were made with bulk products provided by National Enzyme ... Class II
Sep 20, 2013 Serene Science/Source Naturals brand GABA (Gamma-Aminobutyric Acid), CALM MIN... The firm found small piece of metal fragment in one tablet during its inspect... 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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