The Recall Desk
ModerateFDA (Food)·F-2380-2017·Announced 2017-07-19

Source Naturals Hydrogen Boost Capsules Recalled for Undeclared Boron

Source Naturals Hydrogen Boost Capsules are being recalled because they contain low levels of undeclared boron. The recall covers 55,354 units distributed nationwide.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves low levels of undeclared boron, which fits the criteria for moderate severity involving labeling or low-risk contamination issues without reported illness.

Plain-English summary

Threshold Enterprises Ltd is recalling Source Naturals Hydrogen Boost Capsules in 6-count, 30-count, and 60-count bottles. The recall is due to the presence of low levels of undeclared boron in the product. The affected products were manufactured for Source Naturals in Santa Cruz, California.

A total of 55,354 units are included in this recall. The products were distributed nationwide. Specific lot numbers and expiration dates for the 6-count, 30-count, 60-count, and 30+30-count bottles are listed in the official recall documentation.

Consumers should stop using the affected products and check their lot numbers against the list provided by the FDA. The source text does not specify a particular consumer action such as returning the product or seeking a refund, nor does it report any illnesses or injuries associated with the recall.

The recalled product

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
Manufacturer
Threshold Enterprises Ltd
Category
Food — Dietary Supplement
Hazard
Affected units
55,354

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • 30 Count bottles: Lot No. QTY Exp. FG-49254 1
  • 776 01/16 FG-20141 1
  • 500 04/16 FG-26888 1
  • 312 05/17 FG-57329 1
  • 567 04/18 FG-62895 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
  • 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
  • 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
  • 646 08/18 FG-44498 894 08/18 FG-66074 1

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 2 recalled by Threshold Enterprises Ltd under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Related recalls

Same manufacturer · Threshold Enterprises Ltd

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