Herbalife International Of America Inc Recall: Herbalife is recalling Protein Bar-Peanut Butter because it may contain a trace amount of fish gelatin. - F-2239-2017
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.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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?
FDA classifies this recall as Class III. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of July 14, 2017.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.