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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"

Class I - Dangerous
Recalled: October 3, 2025 New York Mutual Trading Seafood

What Should You Do?

  1. Check if you have this product:
    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
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
New York Mutual Trading, Inc.
Reason for Recall:
Undeclared allergen ingredients (fish, soy, and wheat)
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full 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"

Product Codes/Lot Numbers:

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

Distribution:

Distributed in: HI, FL, GA, MA, MD, NJ, NY, PA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: H-0147-2026

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