Vitalicious Acquisition Recall: The affected lots of VitaTops Apple Crumb contain undeclared milk.
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.
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 "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.
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.
