Food recall

Threshold Enterprises Ltd recall: Source Naturals Hydrogen Boost Capsule

Threshold Enterprises Ltd, of Scotts Valley, CA, recalled Source Naturals Hydrogen Boost Capsule and 1 other product. The FDA's reason: “Dietary supplements contain low levels of undeclared boron.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on September 11, 2015, and the FDA first listed it in its Enforcement Report of July 19, 2017. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Other ingredient not on the label (sulfites, dyes...)

Status

Terminated

Closed July 10, 2017

The recall

Company
Threshold Enterprises Ltd (Scotts Valley, CA)
Reason, in FDA's words
“Dietary supplements contain low levels of undeclared boron”
Where it was sold
Nationwide only.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
77531

The 2 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-2380-2017 Class II

    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

    Codes: 30 Count bottles: Lot No. QTY Exp. FG-49254 1,776 01/16 FG-20141 1,500 04/16 FG-26888 1,443 10/16 FG-14566 471 12/16 FG-14806 124 12/16 FG-15403 888 12/16 FG-38154 522 02/14 FG-39838 383 02/14 FG-32297 769 02/14 FG-36649 1,312 05/17 FG-57329 1,567 04/18 FG-62895 1,015 04/18 FG-53250 602 04/18 FG-41921 903 08/18 FG-44178 1,024 08/18 FG-66005 903 04/19 FG-67459 1,101 04/19; 60 count bottles: Lot No. QTY Exp. FG-48012 1,632 01/16 FG-49035 527 01/16 FG-50236 199 01/16 FG-20514 2,268 04/16 FG-23252 21 04/16 FG-25173 1,017 04/16 FG-26889 2,581 10/16 FG-28620 758 10/16 FG-14569 1,006 12/16 FG-15160 1,201 12/16 FG-15161 1,191 12/16 FG-16269 481 12/16 FG-38315 14 02/17 FG-38832 938 02/17 FG-32298 1,886 02/17 FG-33225 650 02/17 FG-36650 1,550 05/17 FG-37372 302 05/17 FG-38672 1,561 05/17 FG-59165 2,675 04/18 FG-57360 2,327 04/18 FG-62847 1,296 04/18 FG-63727 1,019 04/18 FG-53252 722 04/18 FG-54099 929 04/18 FG-54416 845 04/18 FG-45765 658 08/18 FG-50424 161 08/18 FG-41922 1,646 08/18 FG-44498...

    Quantity: 55,354 units

  • F-2383-2017 Class II

    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

    Codes: 30 Count bottles: Lot No. QTY Exp. FG-13852 76 12/15 FG-14726 148 12/15 FG-19274 148 03/16 FG-24304 148 03/16 FG-30636 100 03/16 FG-37569 9 03/16 FG-39616 172 07/17 FG-47423 64 07/17 FG-50614 70 07/17 FG-65266 60 07/17 FG-65266 60 07/17 FG-59256 144 09/18 60 count bottles: Lot No. QTY Exp. FG-13853 338 12/15 FG-14725 468 12/15 FG-19145 290 03/16 FG-23361 206 03/16 FG-23362 396 03/16 FG-34451 98 03/16 FG-38199 38 03/16 FG-39615 424 07/17 FG-50331 122 07/17 FG-53623 144 07/17 FG-59257 362 09/18 FG-65017 206 09/18 120 count bottles: LOT QTY EXP FG-13854 134 12/15 FG-14556 141 12/15 FG-15360 213 12/15 FG-19882 302 03/16 FG-23397 350 03/16 FG-29559 160 03/16 FG-32109 215 03/16 FG-32109 215 03/16 FG-37240 60 03/16 FG-38639 42 03/16 FG-39812 444 07/17 FG-45840 266 07/17 FG-51761 200 07/17 FG-59258 482 09/18 FG-64221 218 09/18 FG-65613 395 09/18; 10 count sample packs; Lot No. QTY Exp. FG-13855 41 12/15 FG-30136 108 03/16 FG-34834 95 03/16 FG-39626 200 07/17 FG-43530 277 07/17 FG-51677 150...

    Quantity: 9,361 units

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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 July 19, 2017.

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.