Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP44302 UPC:8901777282168 Best Before Sept
Summary
The FDA issued a Class I for Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP4 by Vadilal Industries USA Inc.. Reason: Product may be contaminated with Salmonella.
Details
Source
Food Recall
External ID
F-0815-2022
Action Date
2022-03-09
Status
Terminated
Category
food
Product Description
Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP44302 UPC:8901777282168 Best Before September 2023
Lot/Code Info: KWHO Best before Sept 2023 KRQO Best before Sept 2023
Quantity Affected: 997 cases (10 packs/per case)
Reason for Recall
Product may be contaminated with Salmonella
Distribution
Distributed to retail stores nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-20
Company
Newark, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 70 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Vadilal Industries USA Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Vadilal Industries USA Inc. have FDA actions?
This is the only FDA action we have on record for Vadilal Industries USA Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0815-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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