Herbalife International Of America Inc Recall: Herbalife is recalling Protein Bar-Peanut Butter because it may contain a trace amount of fish gelatin.
United States
TerminatedClass III
- Company
- Herbalife International Of America Inc
- Product
- Protein Bar 14 bars/box, Net Wt. 19.74oz (560g) Each ship…
- Recall date
- May 1, 2017
- Terminated
- July 14, 2017
- Source
- FDA
Reason for recall
Herbalife is recalling Protein Bar-Peanut Butter because it may contain a trace amount of fish gelatin.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Protein Bar 14 bars/box, Net Wt. 19.74oz (560g) Each shipping carton contains 12 boxes | Not published in this source record | 55,143 cartons | 066539A11, 066553A11, 066601A11, 066660A11, 066688A11, and 066691A11. |
Distribution
- nationwide in US
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2239-2017
- Event ID
- 77179
- Status
- Terminated
- Classification
- Class III
- Company
- Herbalife International Of America Inc
- Product description
- Protein Bar 14 bars/box, Net Wt. 19.74oz (560g) Each shipping carton contains 12 boxes
- Quantity
- 55,143 cartons
- Reason
- Herbalife is recalling Protein Bar-Peanut Butter because it may contain a trace amount of fish gelatin.
- Recall initiation date
- May 1, 2017
- Report date
- May 24, 2017
- Classification date
- Not published in this source record
- Termination date
- July 14, 2017
- Distribution pattern
- nationwide in US
- UPC, lot, and code information
- 066539A11, 066553A11, 066601A11, 066660A11, 066688A11, and 066691A11.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- 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 Inc
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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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.
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