Joseph Seviroli Inc. Recall: May contain undeclared milk - F-0382-2022
United States
TerminatedClass I
- Company
- Joseph Seviroli Inc.
- Product
- Aplenty Rotini with Plant based Bolognese Meal Kit 24oz
- Recall date
- December 26, 2021
- Terminated
- October 27, 2022
- Source
- FDA
Reason for recall
May contain undeclared milk
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Aplenty Rotini with Plant based Bolognese Meal Kit 24oz | Not published in this source record | 639 cases | Lot 1148 May 28, 2022 Lot 1161 June 10,2022 Lot 1162 June 11, 2022 Item # 19759 UPC # 842379197598 |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0382-2022
- Event ID
- 89304
- Status
- Terminated
- Classification
- Class I
- Company
- Joseph Seviroli Inc.
- Product description
- Aplenty Rotini with Plant based Bolognese Meal Kit 24oz
- Quantity
- 639 cases
- Reason
- May contain undeclared milk
- Recall initiation date
- December 26, 2021
- Report date
- January 19, 2022
- Classification date
- Not published in this source record
- Termination date
- October 27, 2022
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- Lot 1148 May 28, 2022 Lot 1161 June 10,2022 Lot 1162 June 11, 2022 Item # 19759 UPC # 842379197598
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Joseph Seviroli Inc.
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
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of October 27, 2022.
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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