Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut flavor. 14 bars per carton Protein-based snack for energy and n
Summary
The FDA issued a Class II for Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut flavor. 14 bars per car by Herbalife International of America. Reason: Undeclared allergen - egg.
Details
Source
Food Recall
External ID
F-0860-2022
Action Date
2022-03-23
Status
Terminated
Category
food
Product Description
Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut flavor. 14 bars per carton Protein-based snack for energy and nutrition 14 bars 1.23 oz (35 g) each Net wt. 17.3 oz., (490 g) SKU: 0365US Catalog Number: 0365 Formulated and Distributed by Herbalife International of America, Inc. Los Angeles, CA Manufactured by Gustav Berning GmbH & Co., Germany
Lot/Code Info: Lot code G221684A EXP Date 10/2022
Quantity Affected: 13,820 + 23 bars distributed as kits
Reason for Recall
Undeclared allergen - egg
Distribution
Nationwide distribution
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-01
Company
Los Angeles, CA
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 122 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Herbalife International of America 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 (Herbalife International of America) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Herbalife International of America have FDA actions?
Herbalife International of America 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-0860-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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