Oceans Catch All Natural Jonah Crab Combo Meat, Packaged in round plastic containers (tub with snap-on lid), sold refrigerated: 6 ounce, 8 ounce, and 16 ounce

Class I - Dangerous
Recalled: October 24, 2014 Rome Packing Co. Meat & Poultry

What Should You Do?

  1. Check if you have this product:
    6 ounce: lot number 0104791, with a sell by date before 10/13/14; lot number 0104666, with a sell by date before 10/15/14; 8 ounce: lot number 0104787, with a sell by date before 10/14/14; 16 ounce: lot number 0104806, with a sell by date before 10/14/14; lot number 0104845, with a sell by date before 10/16/14
  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:
Rome Packing Co., Inc.
Reason for Recall:
Product may be be contaminated with Listeria monocytogenes.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Oceans Catch All Natural Jonah Crab Combo Meat, Packaged in round plastic containers (tub with snap-on lid), sold refrigerated: 6 ounce, 8 ounce, and 16 ounce

Product Codes/Lot Numbers:

6 ounce: lot number 0104791, with a sell by date before 10/13/14; lot number 0104666, with a sell by date before 10/15/14; 8 ounce: lot number 0104787, with a sell by date before 10/14/14; 16 ounce: lot number 0104806, with a sell by date before 10/14/14; lot number 0104845, with a sell by date before 10/16/14

Distribution:

Distributed in: US, CA, FL, IL, MA, ME, NY, PA, RI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0613-2015

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