Aivia Whey Protein+ Power Herbs Chocolate, NET WT 1.35 LBS (611 G) Manufactured by Nature s Sunshine Products, Inc. 165
Summary
The FDA issued a Class II for Aivia Whey Protein+ Power Herbs Chocolate, NET WT 1.35 LBS (611 G) Manufactured by NATURE'S SUNSHINE PRODUCTS. Reason: Label declares Whey but does not declare Milk..
Details
Source
Food Recall
External ID
F-1540-2022
Action Date
2022-08-17
Status
Terminated
Category
food
Product Description
Aivia Whey Protein+ Power Herbs Chocolate, NET WT 1.35 LBS (611 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street Spanish Fork, Utah 84660. UPC 0 99904 22711 8 Label is read in parts: "***INGREDIENTS: Whey Isolate, Whey Concentration***".
Lot/Code Info: NSP Lot Codes/EXP Date/ Batch #: 001244188 19-May-23 10053964 001247878 8-Jun-23 10054936 001284080 16-Jan-24 10062979 001285198 25-Jan-24 10063351
Quantity Affected: 2,747 bags
Reason for Recall
Label declares Whey but does not declare Milk.
Distribution
Nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-07-22
Company
Lehi, UT
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 31 food recalls issued in the same week, part of 204 food-related FDA actions this month.
NATURE'S SUNSHINE PRODUCTS has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (NATURE'S SUNSHINE PRODUCTS) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does NATURE'S SUNSHINE PRODUCTS have FDA actions?
NATURE'S SUNSHINE PRODUCTS has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1540-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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