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Class II: temporary or reversible health riskTerminated

Vitalab Product packaged in the following ways A) Recall

Product packaged in the following ways A) Sonne's, No

Vitalab Co Inc · Kansas City, MO

Risk level
Class II
Reported by FDA
Mar 14, 2018
Recall ID
F-0883-2018
Check your lot numberHow we source this data

Summary

Vitalab recalled Product packaged in the following ways A) starting Feb 8, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0883-2018 on Mar 14, 2018. Reason: The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label. Status: Terminated.

Why it was recalled

The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.

Product description

Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Sonne's Organic Foods, Inc. N. Kansas City, MO 64116; B) Springreen, No. 87, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Springreen Products, Inc. N. Kansas City, MO 64116;

Lot numbers, UPCs & expiration codes

Lot #s: 12-1-18-1, 02-20-19-1, 02-27-19-2, 06-26-19-3, 08-07-19-4

Where it was sold

Product distributed to consumers, distributors and retailers in the following US states AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, NE, NJ, NY, OH, OR, PA, SD, TN, TX, UT, VA, VT, WA, WI and Canada.

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-0883-2018
Classification
Class II
Status
Terminated
Recall initiated
Feb 8, 2018
FDA report date
Mar 14, 2018
Quantity
1,703 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Vitalab Co Inc

Original FDA data

Every field from FDA enforcement report F-0883-2018, exactly as published.

Show all FDA fields
City
Kansas City
State
MO
Status
Terminated
Country
United States
Event ID
79113
Address
705 Mcgee St
Code information
Lot #s: 12-1-18-1, 02-20-19-1, 02-27-19-2, 06-26-19-3, 08-07-19-4
Postal code
64106-1607
Report date
Mar 14, 2018
Product type
Food
Recall number
F-0883-2018
Classification
Class II
Recalling firm
Vitalab Co Inc
Product quantity
1,703 bottles
Termination date
Jul 24, 2018
Reason for recall
The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Sonne's Organic Foods, Inc. N. Kansas City, MO 64116; B) Springreen, No. 87, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Springreen Products, Inc. N. Kansas City, MO 64116;
Distribution pattern
Product distributed to consumers, distributors and retailers in the following US states AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, NE, NJ, NY, OH, OR, PA, SD, TN, TX, UT, VA, VT, WA, WI and Canada.
Recall initiation date
Feb 8, 2018
Initial firm notification
Letter
Center classification date
Mar 6, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0883-2018, published Mar 14, 2018. View the source record (openFDA) · FDA enforcement reports

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

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