FDA recalls · F-2383-2017
Threshold Enterprises Ltd recall
- FoodSource Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, 60 Count, & 120 Count per bottle; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1750: 60 count Bottle - Product SN1751; 120 count Bottle - Product SN1752; 10 Count Sample Packs - Product SN5024. Manufactured for Source Naturals, Santa Cruz, CA
- ReasonDietary supplements contain low levels of undeclared boron
- ClassClass II: the food could cause temporary or treatable health problems
- StatusClosed by FDA, ended 2017-07-10
- DatesFirm started it 2015-09-11. In FDA's enforcement report 2017-07-19.
- Sold inNationwide only.
- Amount9,361 units
- Codes30 Count bottles: Lot No. QTY Exp. FG-13852 76 12/15 FG-14726 148 12/15 FG-19274 148 03/16 FG-24304 148 03/16 FG-30636 100 03/16 FG-37569 9 03/16 FG-39616 172 07/17 FG-47423 64 07/17 FG-50614 70 07/17 FG-65266 60 07/17 FG-65266 60 07/17 FG-59256 144 09/18 60 count bottles: Lot No. QTY Exp. FG-13853 338 12/15 FG-14725 468 12/15 FG-19145 290 03/16 FG-23361 206 03/16 FG-23362 396 03/16 FG-34451 98 03/16 FG-38199 38 03/16 FG-39615 424 07/17 FG-50331 122 07/17 FG-53623 144 07/17 FG-59257 362 09/18 FG-65017 206 09/18 120 count bottles: LOT QTY EXP FG-13854 134 12/15 FG-14556 141 12/15 FG-15360 213 12/15 FG-19882 302 03/16 FG-23397 350 03/16 FG-29559 160 03/16 FG-32109 215 03/16 FG-32109 215 03/16 FG-37240 60 03/16 FG-38639 42 03/16 FG-39812 444 07/17 FG-45840 266 07/17 FG-51761 200 07/17 FG-59258 482 09/18 FG-64221 218 09/18 FG-65613 395 09/18; 10 count sample packs; Lot No. QTY Exp. FG-13855 41 12/15 FG-30136 108 03/16 FG-34834 95 03/16 FG-39626 200 07/17 FG-43530 277 07/17 FG-51677 150 07/17 FG-59259 362 09/18
- FirmThreshold Enterprises Ltd, Scotts Valley, CA · Voluntary: Firm initiated
Products we list
None. We tie a recall to a product only by a barcode printed in the recall, and this one names none we list. That does not mean the recalled food is missing from our listings.
From FDA's enforcement report, via openFDA (CC0): raw data for this recall. FDA's own Enforcement Report search finds it by its number, F-2383-2017. Class meanings: FDA.