Paras Premium Golden Raisins; 7 oz and 14 oz; INGREDIENTS: RAISINS; ALLERGEN STATEMENT: Processed in a gluten-free and p
Summary
The FDA issued a Class I for Paras Premium Golden Raisins; 7 oz and 14 oz; INGREDIENTS: RAISINS; ALLERGEN STA by Apna Wholesale Inc.. Reason: Product contains undeclared sulfites (56.8mg/serving).
Details
Source
Food Recall
External ID
F-0564-2025
Action Date
2025-02-26
Status
Terminated
Category
food
Product Description
Paras Premium Golden Raisins; 7 oz and 14 oz; INGREDIENTS: RAISINS; ALLERGEN STATEMENT: Processed in a gluten-free and peanut-free plant; UPC: 818051014811 and 818051014828
Lot/Code Info: UPC only - see Product Description.
Quantity Affected: 598 cases
Reason for Recall
Product contains undeclared sulfites (56.8mg/serving)
Distribution
NY and MA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-07
Company
Hicksville, NY
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 37 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 (Apna Wholesale Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Apna Wholesale Inc. have FDA actions?
This is the only FDA action we have on record for Apna Wholesale Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0564-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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