Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; ...
FDA Recall #F-2380-2017 — Class II — September 11, 2015
Recall Summary
| Recall Number | F-2380-2017 |
| Date Initiated | September 11, 2015 |
| Classification | Class II |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Threshold Enterprises Ltd |
| Location | Scotts Valley, CA |
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
Reason for Recall
Dietary supplements contain low levels of undeclared boron
Classification
Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution Pattern
Nationwide only.
Product Quantity
55,354 units
Product Codes / Lot Numbers
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
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.
Frequently Asked Questions
Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.
If you have a food allergy and consumed the recalled product, monitor yourself closely for allergic reaction symptoms — including hives, swelling, difficulty breathing, nausea, vomiting, or anaphylaxis. If you experience any symptoms, seek medical attention immediately. For anaphylaxis (severe allergic reaction with difficulty breathing, rapid heartbeat, or loss of consciousness), call 911 and use an epinephrine auto-injector (EpiPen) if available. Stop consuming the product and check all products from the same manufacturer for similar labeling issues, as undeclared allergens sometimes affect multiple products from the same production facility.
Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.
The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.