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Class II: temporary or reversible health riskTerminated

Threshold Enterprises Source Naturals Hydrogen Boost Capsule: 6 Recall

Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count

Threshold Enterprises Ltd · Scotts Valley, CA

Risk level
Class II
Reported by FDA
Jul 19, 2017
Recall ID
F-2380-2017
Check your lot numberHow we source this data

Summary

Threshold Enterprises recalled Source Naturals Hydrogen Boost Capsule: 6 starting Sep 11, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2380-2017 on Jul 19, 2017. Reason: Dietary supplements contain low levels of undeclared boron. Status: Terminated.

Why it was recalled

Dietary supplements contain low levels of undeclared boron

Product description

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

Lot numbers, UPCs & expiration 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 894 08/18 FG-66074 1,634 04/19 FG-66073 2,953 04/19; 6 count trial bottles: LOT QTY EXP FG-50276 70 01/16 FG-20144 197 04/16 FG-27249 72 10/16 FG-14807 130 12/16 FG-32299 180 02/17 FG-36648 260 05/17 FG-57331 139 04/18 FG-46406 77 08/18 FG-67263 140 04/19; 30 + 30 Count Bottles; FG-20143 74 04/16 FG-14590 14 12/16 FG-45766 62 08/18 FG-44258 32 08/18 FG-66279 62 04/19

Where it was sold

Nationwide only.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2380-2017
Classification
Class II
Status
Terminated
Recall initiated
Sep 11, 2015
FDA report date
Jul 19, 2017
Quantity
55,354 units
Recall type
Voluntary: Firm initiated
Recalling firm
Threshold Enterprises Ltd

Original FDA data

Every field from FDA enforcement report F-2380-2017, exactly as published.

Show all FDA fields
City
Scotts Valley
State
CA
Status
Terminated
Country
United States
Event ID
77531
Address
23 Janis Way
Code information
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 894 08/18 FG-66074 1,634 04/19 FG-66073 2,953 04/19; 6 count trial bottles: LOT QTY EXP FG-50276 70 01/16 FG-20144 197 04/16 FG-27249 72 10/16 FG-14807 130 12/16 FG-32299 180 02/17 FG-36648 260 05/17 FG-57331 139 04/18 FG-46406 77 08/18 FG-67263 140 04/19; 30 + 30 Count Bottles; FG-20143 74 04/16 FG-14590 14 12/16 FG-45766 62 08/18 FG-44258 32 08/18 FG-66279 62 04/19
Postal code
95066-3506
Report date
Jul 19, 2017
Product type
Food
Recall number
F-2380-2017
Classification
Class II
Recalling firm
Threshold Enterprises Ltd
Product quantity
55,354 units
Termination date
Jul 10, 2017
Reason for recall
Dietary supplements contain low levels of undeclared boron
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
Nationwide only.
Recall initiation date
Sep 11, 2015
Initial firm notification
Telephone
Center classification date
Jul 10, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2380-2017, published Jul 19, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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