Data Foundry

Food recalls 2017

Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack — Class II food recall F-2383-2017

Terminated recall by Threshold Enterprises Ltd, reported 2017-07-19, distributed nationwide. Dietary supplements contain low levels of undeclared boron

Recall numberF-2383-2017
Product typeFood
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmThreshold Enterprises Ltd, Scotts Valley, CA, United States
Recall initiated2015-09-11
Classified2017-07-10
Reported by FDA2017-07-19
Terminated2017-07-10
DistributedNationwide (US)
Quantity9,361 units
Reason classesundeclared allergen
Lot numbers03/16, 07/17, 09/18, 100, 108, 12/15, 120, 122, 134, 141, 144, 148, 150, 160, 172, 200, 206, 213, 215, 218, 266, 277, 290, 302, 338, 350, 362, 395, 396, 424, 444, 468, 482, FG-13852, FG-13853, FG-13854, FG-13855, FG-14556, FG-14725, FG-14726 and 38 more

Product

Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, 60 Count, & 120 Count per bottle; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1750: 60 count Bottle - Product SN1751; 120 count Bottle - Product SN1752; 10 Count Sample Packs - Product SN5024. 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-2383-2017. 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.