50%

Fewer recalls than
Supplements & Specialty peers

Threshold Enterprises — FDA Recall History & Enforcement Records

Established Player · Supplements & Specialty

Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.

As of July 16, 2026, Threshold Enterprises has 8 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 10 Sep 2019. Threshold Enterprises is categorized under Supplements & Specialty based on their predominant recall history.

8
Total FDA recalls
12.8
Years in FDA database
0.6
Recalls per year
2,501 days(6.8 yrs)
Since last recall
0.0%
Class I (life-threatening)
0.6 recalls/yr vs Supplements & Specialty avg 2.3/yrWell Below Average

Recall activity over time for Threshold Enterprises

How serious are Threshold Enterprises recalls?

FDA recall classifications by severity

Class I (Life-threatening)
0.0% (0 recalls)
Class II (Moderate risk)
87.5% (7 recalls)
Class III (Minor violation)
12.5% (1 recalls)

Full FDA recall history for Threshold Enterprises

All 8 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first

Date Product Reason Class & Status
10 Sep 2019Official FDA Notice Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets, 60 tablets Manufactured for Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation. Class IIITerminated
7 Dec 2018Official FDA Notice Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF0003; 90 count – Item number PF0002; 180 count Recall of Mullein Lung Complex due to a labeling error which indicates the incorrect excipient profile (inactive ingredients). Class IITerminated
16 Jun 2017Official FDA Notice Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 6 Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth. Class IITerminated
12 Dec 2016Official FDA Notice Source Naturals Dietary Supplement Vitamin D-3; Bioactive Form for Bone and Immune Health 2000 IU per serving, 500% Testing of Vitamin D-3 as a result of a consumer complaint found specific lots to have lower concentrations than product specifications of ingredient Class IITerminated
11 Sep 2015Official FDA Notice Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; Ingredient: Maltodextrin, Cellulose (Capsu Dietary supplements contain low levels of undeclared boron Class IITerminated
11 Sep 2015Official FDA Notice Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, 60 Count, & 120 Count per bottle; Ingredie Dietary supplements contain low levels of undeclared boron Class IITerminated
22 Nov 2013Official FDA Notice Source Naturals Essential Enzyme Ultra VEGI-CAP: Premium Digestive Enzyme Blend; 30, 60, 90 & 120 count bottles. Veg Dietary Supplements were made with bulk products provided by National Enzyme Company which are currently under recall for chloramphenicol Class IITerminated
20 Sep 2013Official FDA Notice Serene Science/Source Naturals brand GABA (Gamma-Aminobutyric Acid), CALM MIND, A dietary supplement, 45 Tablets, Item The firm found small piece of metal fragment in one tablet during its inspection process. Class IITerminated

Where have Threshold Enterprises recalls occurred?

States affected across all recorded FDA enforcement actions

Nationwide

Where does this recall data come from?

Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.

Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.

To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.

© 2026 FoodRecallFinder.com | Turnkey Trading Unlimited LLC. All rights reserved. FDA recall data sourced from openFDA.gov.

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