Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 11, 2015 (11 years ago)

Source Naturals Hydrogen Boost Capsule recall

Recalled by Threshold Enterprises Ltd · Scotts Valley, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Dietary supplements contain low levels of undeclared boron

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

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

Quantity: 55,354 units

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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.

FDA's distribution note: Nationwide only.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Threshold Enterprises Ltd
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 11, 2015
In FDA report of
Jul 19, 2017
Terminated
Jul 10, 2017
FDA recall number
F-2380-2017 · event 77531
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

Other recalls by Threshold Enterprises Ltd

Class II · Moderate risk Terminated Labeling

Planetary Herbals Mullein Lung Complex

Reason Recall of Mullein Lung Complex due to a labeling error which indicates the incorrect excipient profile (inactive ingredients).

Threshold Enterprises Ltd Nationwide F-1097-2019
Class II · Moderate risk Terminated Other

Planetary Herbals Ginseng Classic

Reason Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.

Threshold Enterprises Ltd 7 states F-3338-2017
Class II · Moderate risk Terminated Labeling

Source Naturals Dietary Supplement Vitamin D-3

Reason Testing of Vitamin D-3 as a result of a consumer complaint found specific lots to have lower concentrations than product specifications of ingredient labeling.

Threshold Enterprises Ltd Nationwide F-2178-2017