FDA Recall United States TerminatedTerminated: July 10, 2017Historical recordClass II
Threshold Enterprises Ltd
- Product
- Source Naturals Renewal Antioxidant Tablet: 10 Count Sample…
- Published
- July 19, 2017
- Distribution
- Nationwide
Threshold Enterprises Ltd Recall: Dietary supplements contain low levels of undeclared boron - F-2380-2017
United States
TerminatedClass II
- Company
- Threshold Enterprises Ltd
- Product
- Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30…
- Recall date
- September 11, 2015
- Terminated
- July 10, 2017
- Source
- FDA
Reason for recall
Dietary supplements contain low levels of undeclared boron
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 55,354 units | 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 |
Distribution
- Nationwide only.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2380-2017
- Event ID
- 77531
- Status
- Terminated
- Classification
- Class II
- Company
- Threshold Enterprises Ltd
- 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
- Quantity
- 55,354 units
- Reason
- Dietary supplements contain low levels of undeclared boron
- Recall initiation date
- September 11, 2015
- Report date
- July 19, 2017
- Classification date
- Not published in this source record
- Termination date
- July 10, 2017
- Distribution pattern
- Nationwide only.
- UPC, lot, and 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
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 77531 with 1 other product entry in Public Health Trace.
Responsible company: Threshold Enterprises Ltd
Other recalls from Threshold Enterprises Ltd
FDA Recall United States TerminatedTerminated: February 3, 2020Historical recordClass III
Threshold Enterprises Ltd
- Product
- Source Naturals Dietary Supplement Brain Charge Advanced…
- Published
- October 30, 2019
- Distribution
- U.S. distribution to the following: AL,…
FDA Recall United States TerminatedTerminated: June 7, 2019Historical recordClass II
Threshold Enterprises Ltd
- Product
- Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count,…
- Published
- March 6, 2019
- Distribution
- Nationwide
FDA Recall United States TerminatedTerminated: August 2, 2017Historical recordClass II
Threshold Enterprises Ltd
- Product
- Planetary Herbals Ginseng Classic; Classic Chinese Energize…
- Published
- August 9, 2017
- Distribution
- CA, MN, WA, IL, PR, ME, SD.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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Technical source data
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Frequently asked questions
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How to interpret this historical record
This record is preserved as published by FDA, as of July 10, 2017.
Status as reported: Terminated.
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