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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 I

Dangerous 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

  1. Initiated
    Oct 3, 2025
  2. Published
    Nov 12, 2025
  3. Terminated
    Apr 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.