Vadilal Industries USA Inc. Recall: Product may be contaminated with Salmonella
United States
TerminatedClass I
- Company
- Vadilal Industries USA Inc.
- Product
- Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz…
- Recall date
- February 20, 2022
- Terminated
- July 22, 2022
- Source
- FDA
Reason for recall
Product may be contaminated with Salmonella
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP44302 UPC:8901777282168 Best Before September 2023 | 8901777282168 | 997 cases (10 packs/per case) | KWHO Best before Sept 2023 KRQO Best before Sept 2023 |
Distribution
- Distributed to retail stores nationwide.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0815-2022
- Event ID
- 89630
- Status
- Terminated
- Classification
- Class I
- Company
- Vadilal Industries USA Inc.
- Product description
- Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP44302 UPC:8901777282168 Best Before September 2023
- Quantity
- 997 cases (10 packs/per case)
- Reason
- Product may be contaminated with Salmonella
- Recall initiation date
- February 20, 2022
- Report date
- March 9, 2022
- Classification date
- Not published in this source record
- Termination date
- July 22, 2022
- Distribution pattern
- Distributed to retail stores nationwide.
- UPC, lot, and code information
- UPC 8901777282168; KWHO Best before Sept 2023 KRQO Best before Sept 2023
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Vadilal Industries USA 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?
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?
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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 July 22, 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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