Food recalls by company
Threshold Enterprises Ltd food recalls
The FDA has listed 7 food recalls by Threshold Enterprises Ltd since its Enforcement Reports began in June 2012, the newest on October 30, 2019. 0 were Class I, the most serious kind. The most common reason: labeling, packaging or manufacturing problems (3).
Food recalls since 2012
7
Class I, the most serious
0
Newest
October 30, 2019
Every recall, newest first
By the date the FDA first listed each in its weekly Enforcement Report. Each recall's page lists every product, with the codes that tell whether a package is part of it.
2019 (2 recalls)
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Class III Terminated
Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets
Why: Labeling, packaging or manufacturing problems
“Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation.”
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Class II Terminated
Planetary Herbals Mullein Lung Complex
Why: Labeling, packaging or manufacturing problems
“Recall of Mullein Lung Complex due to a labeling error which indicates the incorrect excipient profile (inactive ingredients).”
2017 (3 recalls)
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Class II Terminated
Planetary Herbals Ginseng Classic
Why: Other germs or toxins (botulism, hepatitis A, mold...)
“Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.”
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Class II Terminated
Source Naturals Hydrogen Boost Capsule (2 products)
Why: Other ingredient not on the label (sulfites, dyes...)
“Dietary supplements contain low levels of undeclared boron”
-
Class II Terminated
Source Naturals Dietary Supplement Vitamin D-3
Why: Labeling, packaging or manufacturing problems
“Testing of Vitamin D-3 as a result of a consumer complaint found specific lots to have lower concentrations than product specifications of ingredient labeling.”
2013 (2 recalls)
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Class II Terminated
Source Naturals Essential Enzyme Ultra VEGI-CAP
“Dietary Supplements were made with bulk products provided by National Enzyme Company which are currently under recall for chloramphenicol”
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Class II Terminated
Serene Science/Source Naturals brand GABA (Gamma-Aminobutyric Acid), CALM MIND, A dietary supplement
Why: Metal, plastic, glass or other objects
“The firm found small piece of metal fragment in one tablet during its inspection process.”
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Recalls are grouped by the company name the FDA lists as the recalling firm, so a company's other names, or a parent company's brands, may have pages of their own. A recall is listed once however many products it covers.
Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of October 14, 2026.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.