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

Source Naturals Renewal Antioxidant Tablet 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 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

Quantity: 9,361 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-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

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-2383-2017 · 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