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Herbalife International of America Recall: Undeclared allergen - egg

United States

TerminatedClass II

Company
Herbalife International of America
Product
Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut fla…
Recall date
March 1, 2022
Terminated
April 15, 2022
Source
FDA

Reason for recall

Undeclared allergen - egg

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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 Not published in this source record 13,820 + 23 bars distributed as kits Lot code G221684A EXP Date 10/2022

Distribution

  • Nationwide distribution

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0860-2022
Event ID
89674
Status
Terminated
Classification
Class II
Company
Herbalife International of America
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
Quantity
13,820 + 23 bars distributed as kits
Reason
Undeclared allergen - egg
Recall initiation date
March 1, 2022
Report date
March 23, 2022
Classification date
Not published in this source record
Termination date
April 15, 2022
Distribution pattern
Nationwide distribution
UPC, lot, and code information
Lot code G221684A EXP Date 10/2022
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Herbalife International of America

Other recalls from Herbalife International of America

FDA Recall United States Terminated Historical recordClass II

Herbalife International of America

Product
Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) U…
Published
July 30, 2025
Distribution
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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.