TOJI CO. Recall: Undeclared allergen ingredient (fish)
United States
OngoingClass II
- Company
- TOJI CO.
- Product
- Cloud Cafe branded Collagen Milk; Strawberry Milk Zero; Caff…
- Recall date
- September 15, 2026
- Source
- FDA
Reason for recall
Undeclared allergen ingredient (fish)
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Cloud Cafe branded Collagen Milk; Strawberry Milk Zero; Caffeine Free; 10pc/box | Not published in this source record | 820 boxes | OB25001; Best By: 5/13/2028 |
Distribution
- Product was sold to a single distributor located in Los Angeles.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-1400-2026
- Event ID
- 99929
- Status
- Ongoing
- Classification
- Class II
- Company
- TOJI CO.
- Product description
- Cloud Cafe branded Collagen Milk; Strawberry Milk Zero; Caffeine Free; 10pc/box
- Quantity
- 820 boxes
- Reason
- Undeclared allergen ingredient (fish)
- Recall initiation date
- September 15, 2026
- Report date
- October 7, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Product was sold to a single distributor located in Los Angeles.
- UPC, lot, and code information
- OB25001; Best By: 5/13/2028
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: TOJI CO.
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.
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 "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.
