Food FDA Class I Terminated Undeclared allergen
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#
New York Mutual Trading, Inc. Published Nov 12, 2025
Risk level
Class IDangerous or defective — could cause serious health problems or death.
Severity score 87/100
What should you do?
- Check whether you have this product, using the lot codes, UPCs, and dates listed below.
- If you are allergic or sensitive to the ingredient noted, do not eat it — it could cause a serious reaction.
- Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
- Contact New York Mutual Trading, Inc. or your place of purchase with questions, and see the source record below for full details.
Reason for recall
Undeclared allergen ingredients (fish, soy, and wheat)
Hazards
Fish · primarySoybeans Wheat
Affected products (1)
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"
~ 21 cases across both recalled products
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
Affected areas
FloridaGeorgiaHawaiiMarylandMassachusettsNew JerseyNew YorkPennsylvania
Timeline
- InitiatedOct 3, 2025
- PublishedNov 12, 2025
- TerminatedApr 21, 2026
- Recall number
- H-0147-2026
- Agency
- U.S. Food and Drug Administration
- Country
- US
FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.