Source Naturals Hydrogen Boost Capsule: 6 Count Trial — Class II food recall F-2380-2017
Terminated recall by Threshold Enterprises Ltd, reported 2017-07-19, distributed nationwide. Dietary supplements contain low levels of undeclared boron
| Recall number | F-2380-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Threshold Enterprises Ltd, Scotts Valley, CA, United States |
| Recall initiated | 2015-09-11 |
| Classified | 2017-07-10 |
| Reported by FDA | 2017-07-19 |
| Terminated | 2017-07-10 |
| Distributed | Nationwide (US) |
| Quantity | 55,354 units |
| Reason classes | undeclared allergen |
| Lot numbers | 006, 01/16, 015, 017, 019, 02/14, 02/17, 024, 04/16, 04/18, 04/19, 05/17, 08/18, 10/16, 101, 12/16, 124, 130, 139, 140, 161, 180, 191, 197, 199, 201, 260, 268, 296, 302, 312, 327, 383, 443, 471, 481, 500, 522, 527, 550 and 80 more |
Product
Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1855: 60 count Bottle - Product SN1856; 6 count Bottle - Product SN2314; 30 count + 30 count bottle - Product SN7171 Manufactured for Source Naturals, Santa Cruz, CA
Reason for recall
Dietary supplements contain low levels of undeclared boron
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-2380-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.