NAFCO, WHITING FILLET SKIN-ON BONELESS IQF, 2 lb., Cases are corrugate. The product is individually frozen and packed in
Summary
The FDA issued a Class III for NAFCO, WHITING FILLET SKIN-ON BONELESS IQF, 2 lb., Cases are corrugate. The prod by Stanley Pearlman Enterprises, Inc.. Reason: Recall initiated due to the wrong best by date (1-11-2025) being printed on the retail bag which would imply that these are expired but in truth they .
Details
Source
Food Recall
External ID
H-0641-2025
Action Date
2025-10-08
Status
Terminated
Category
food
Product Description
NAFCO, WHITING FILLET SKIN-ON BONELESS IQF, 2 lb., Cases are corrugate. The product is individually frozen and packed in food contact retail bag. 15 bags per case. Keep Frozen
Lot/Code Info: Lot# 2501032 Best By Date: 1/11/25
Quantity Affected: 141 cases / 2115 bags
Reason for Recall
Recall initiated due to the wrong best by date (1-11-2025) being printed on the retail bag which would imply that these are expired but in truth they are good until 1-11-2027.
Distribution
The product was distributed to the following states, MD, PA .
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-15
Company
Jessup, MD
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 39 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Stanley Pearlman Enterprises, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Stanley Pearlman Enterprises, Inc. have FDA actions?
This is the only FDA action we have on record for Stanley Pearlman Enterprises, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0641-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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