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Class II: temporary or reversible health riskTerminated

Threshold Enterprises Source Naturals Dietary Supplement Vitamin Recall

Source Naturals Dietary Supplement Vitamin D-3

Threshold Enterprises Ltd · Scotts Valley, CA

Risk level
Class II
Reported by FDA
May 10, 2017
Recall ID
F-2178-2017
Check your lot numberHow we source this data

Summary

Threshold Enterprises recalled Source Naturals Dietary Supplement Vitamin starting Dec 12, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2178-2017 on May 10, 2017. 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. Status: Terminated.

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.

Product description

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.

Lot numbers, UPCs & expiration codes

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2178-2017
Classification
Class II
Status
Terminated
Recall initiated
Dec 12, 2016
FDA report date
May 10, 2017
Quantity
129,331 total units
Recall type
Voluntary: Firm initiated
Recalling firm
Threshold Enterprises Ltd

Original FDA data

Every field from FDA enforcement report F-2178-2017, exactly as published.

Show all FDA fields
City
Scotts Valley
State
CA
Status
Terminated
Country
United States
Event ID
77114
Address
23 Janis Way
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.
Postal code
95066-3506
Report date
May 10, 2017
Product type
Food
Recall number
F-2178-2017
Classification
Class II
Recalling firm
Threshold Enterprises Ltd
Product quantity
129,331 total units
Termination date
May 3, 2017
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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.
Distribution pattern
Nationwide
Recall initiation date
Dec 12, 2016
Initial firm notification
Telephone
Center classification date
May 3, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2178-2017, published May 10, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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