Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77114

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
December 12, 2016
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Threshold Enterprises Ltd

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

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.

F-2178-2017
Recall number
F-2178-2017
Initiated
December 12, 2016
Classification
Class II
Status
Terminated
Recalling firm
Threshold Enterprises Ltd
Quantity
129,331 total units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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.

Code information

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.

Distribution pattern

Nationwide