Bumble Bee Brand 5oz Chunk White Albacore in Water

Class I - Dangerous
Recalled: March 1, 2013 Bumble Bee International Beverages Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Code & Best By Date 3016SA2CKP 1/16/2016 3016SA3CKP 1/16/2016 3016SA4CKP 1/16/2016 3017SA1CKP 1/17/2016 3017SA2CKP 1/17/2016 3017SA3CKP 1/17/2016 3017SA4CKP 1/17/2016 3017SA5CKP 1/17/2016 3017SADCKP 1/17/2016 3017SAECKP 1/17/2016 3017SAFCKP 1/17/2016 3017SABCKP 1/17/2016 3017SAACKP 1/17/2016 3017SACCKP 1/17/2016 3017SB2.CKP 1/17/2016
  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:
Bumble Bee International
Reason for Recall:
Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of 5-ounce Chunk White Albacore and Chunk Light Tuna products. The recall has been issued because the products do not meet the companys standards for seal tightness.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Bumble Bee Brand 5oz Chunk White Albacore in Water

Product Codes/Lot Numbers:

Lot Code & Best By Date 3016SA2CKP 1/16/2016 3016SA3CKP 1/16/2016 3016SA4CKP 1/16/2016 3017SA1CKP 1/17/2016 3017SA2CKP 1/17/2016 3017SA3CKP 1/17/2016 3017SA4CKP 1/17/2016 3017SA5CKP 1/17/2016 3017SADCKP 1/17/2016 3017SAECKP 1/17/2016 3017SAFCKP 1/17/2016 3017SABCKP 1/17/2016 3017SAACKP 1/17/2016 3017SACCKP 1/17/2016 3017SB2.CKP 1/17/2016

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1290-2013

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