Perfect Day Inc Recall: Presence of coliform found in 3rd party lab samples
United States
TerminatedClass III
- Company
- Perfect Day Inc
- Product
- Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwic…
- Recall date
- November 2, 2022
- Terminated
- February 6, 2023
- Source
- FDA
Reason for recall
Presence of coliform found in 3rd party lab samples
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 oz (2.9 oz./unit) UPC: 8 5000988328 5 Distributed by Coolhaus 8688 Washington Blvd. Culver City, CA 90232 | Not published in this source record | 284 cases | Best By Date: 3/19/2024 |
Distribution
- Product was shipped only to consignee
- KeHE Distributors
- with locations in TX
- MD
- CO
- and CA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0179-2023
- Event ID
- 91118
- Status
- Terminated
- Classification
- Class III
- Company
- Perfect Day Inc
- Product description
- Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 oz (2.9 oz./unit) UPC: 8 5000988328 5 Distributed by Coolhaus 8688 Washington Blvd. Culver City, CA 90232
- Quantity
- 284 cases
- Reason
- Presence of coliform found in 3rd party lab samples
- Recall initiation date
- November 2, 2022
- Report date
- December 7, 2022
- Classification date
- Not published in this source record
- Termination date
- February 6, 2023
- Distribution pattern
- Product was shipped only to consignee, KeHE Distributors, with locations in TX, MD, CO, and CA
- UPC, lot, and code information
- Best By Date: 3/19/2024
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Perfect Day Inc
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Texas | 1 |
| Maryland | 1 |
| Colorado | 1 |
| California | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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?
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.
Official guidance and record verification
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How to interpret this historical record
This record is preserved as published by FDA, as of February 6, 2023.
Status as reported: Terminated.
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