Frozen Crab Paste; 3.5 OZ (100g); Imported by Mutual Tading Co. Inc. UPC# 72546723040 "Not for retail Sale" Frozen Crab
Summary
The FDA issued a Class I for Frozen Crab Paste; 3.5 OZ (100g); Imported by Mutual Tading Co. Inc. UPC# 72546 by New York Mutual Trading, Inc.. Reason: Undeclared allergen ingredients (fish, soy, and wheat).
Details
Source
Food Recall
External ID
H-0147-2026
Action Date
2025-11-12
Status
Terminated
Category
food
Product Description
Frozen Crab Paste; 3.5 OZ (100g); Imported by Mutual Tading Co. Inc. UPC# 72546723040 "Not for retail Sale" Frozen Crab Paste IM-2 in w/Tray; 500g; Imported by Mutual Trading Co. Inc. UPC# 72546607852 "Not for retail Sale" Frozen Crab Paste; 17.6 OZ (500g); Imported by Mutual Tading Co. Inc. UPC# 72546607852 "Not for retail Sale"
Lot/Code Info: Expiration Dates for 3.5 oz: 2025.11.10; 2026.02.09; 2026.03.09; 2026.05.26; 2026.06.20 Expiration Dates for 500g: 2026.05.12
Quantity Affected: ~ 21 cases across both recalled products
Reason for Recall
Undeclared allergen ingredients (fish, soy, and wheat)
Distribution
Products were labeled "not for retail sale" and were distributed to various restaurants across HI, FL, GA, MA, MD, NJ, NY, PA.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-03
Company
Secaucus, 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 34 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 (New York Mutual Trading, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does New York Mutual Trading, Inc. have FDA actions?
This is the only FDA action we have on record for New York Mutual Trading, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0147-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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