Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 12, 2016 (10 years ago)

Source Naturals Dietary Supplement Vitamin D-3 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

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.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Source Naturals Dietary Supplement Vitamin D-3; Bioactive Form for Bone and Immune Health 2000 IU per serving, 500% DV. Other ingredients: Vegetable Glycerin, Deionized water, citric acid, Natural orange flavor and lemon essential oil. Use 5 drops once daily in a drink. Packed in glass bottles in the following sizes: Unit Size 1 fl. oz. (29.57 mL), UPC 0 21078 02274 9; 2 fl. oz. (59.14 mL) - UPC 0 21078 02275 6 4 fl. oz. (118.28 mL), UPC 0 21078 02276 3 glass bottles: Codes: 1 ounce glass bottle: SN2274; XUB078; 2 ounce glass bottle: SN2275; 4 ounce glass bottle: SN2276. Manufactured for: Source Naturals, Santa Cruz, CA.

Quantity: 129,331 total units

Food: Dietary supplements

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.

Lot number/expiry date SN22274: 1 oz bottle: FG-77168, 03/19; FG-72299, 09/18; FG-73645, 09/18; FG-63547, 01/18; FG-55486, 08/17; FG-55923, 08/17; FG-59576, 08/17. XUB078: 1 oz. bottle: FG-77171, 03/19; FG-77172, 03/19; FG-77173, 03/19; FG-79391; 03/19; FG-72190, 09/18; FG-72444, 09/18; FG-73746, 09/18; FG-62593, 01/18; FG-64694, 01/18; FG-55489, 08/17; FG-56655, 08/17; FG-57122, 08/17; FG-59131, 08/17. SN2275 - 2 oz. bottle: FG-77169, 03/19; FG-72330, 09/18; FG-73644, 09/18; FG-74819, 09/18; FG-62810, 01/18; FG-65424, 01/18; FG-67336, 01/18; FG-70958, 01/18; FG-71903, 01/18; FG-55487, 08/17; FG-57284, 08/17; FG-57284, 08/17; FG-62591, 08/17. SN2276 - 4 oz. bottle: FG-77170, 03/19; FG-72301, 09/18; FG-74822, 09/18; FG-62834, 01/18; FG-66128, 01/18; FG-69301, 01/18; FG-71174, 01/18; FG-55488, 08/17; FG-57224, 08/17; FG-58614, 08/17; FG-60671, 08/17; FG-61698, 08/17.

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

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
Dec 12, 2016
In FDA report of
May 10, 2017
Terminated
May 3, 2017
FDA recall number
F-2178-2017 · event 77114
Official record
FDA enforcement report search

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

Recent dietary supplements recalls

All dietary supplements recalls