Honeyville, Inc Recall: Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.
United States
OngoingClass I
- Company
- Honeyville, Inc
- Product
- (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote…
- Recall date
- April 21, 2026
- Source
- FDA
Reason for recall
Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099 | Not published in this source record | 4980 pounds (all on hold at customer location) | Lot number# 0325357B201 |
Distribution
- Distribution is to California and Utah consignees.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0849-2026
- Event ID
- 98841
- Status
- Ongoing
- Classification
- Class I
- Company
- Honeyville, Inc
- Product description
- (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099
- Quantity
- 4980 pounds (all on hold at customer location)
- Reason
- Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.
- Recall initiation date
- April 21, 2026
- Report date
- June 3, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Distribution is to California and Utah consignees.
- UPC, lot, and code information
- Lot number# 0325357B201
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Honeyville, 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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." 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.
