Vitalicious Acquisition Recall: The affected lots of VitaTops Apple Crumb contain undeclared milk. - F-0370-2017
United States
TerminatedClass I
- Company
- Vitalicious Acquisition
- Product
- VitaTops Apple Crumb, NET WT. 2 oz. (55g), packed in a clear…
- Recall date
- April 21, 2016
- Terminated
- April 17, 2017
- Source
- FDA
Reason for recall
The affected lots of VitaTops Apple Crumb contain undeclared milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| VitaTops Apple Crumb, NET WT. 2 oz. (55g), packed in a clear plastic film and sold frozen in cases of 12 units, 24 units, or variety packs. The affected lots were sold in case of 24 units per case. | Not published in this source record | 145 cases (24 units per case) | Lots 16 075 C and 16 078 C (stamped on top of film) |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0370-2017
- Event ID
- 73970
- Status
- Terminated
- Classification
- Class I
- Company
- Vitalicious Acquisition
- Product description
- VitaTops Apple Crumb, NET WT. 2 oz. (55g), packed in a clear plastic film and sold frozen in cases of 12 units, 24 units, or variety packs. The affected lots were sold in case of 24 units per case.
- Quantity
- 145 cases (24 units per case)
- Reason
- The affected lots of VitaTops Apple Crumb contain undeclared milk.
- Recall initiation date
- April 21, 2016
- Report date
- November 9, 2016
- Classification date
- Not published in this source record
- Termination date
- April 17, 2017
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- Lots 16 075 C and 16 078 C (stamped on top of film)
- 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: Vitalicious Acquisition
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.
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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?
FDA classifies this recall as Class I. 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
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How to interpret this historical record
This record is preserved as published by FDA, as of April 17, 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.
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