Daily Chef Peanut Butter Bars, Net Wt. 27 oz (1 lb 11 oz) 765g, Made in Canada, Manufactured for: CSM Bakery Products NA, Inc., Tucker, GA 30084

Class I - Dangerous
Recalled: September 23, 2015 CSM Bakery Products NA Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    UPC Code: 78742 11172, Lot: TFF 15 237, Shipper Best By Code: Aug 25, 2016; Lot: TFF 15 238, Shipper Best By Code: Aug 26, 2016; Lot: TFF 15 239, Shipper Best By Code: Aug 27, 2016, Lot: TFF 15 226, Shipper Best By Code: Aug 14, 2016; Lot: TFF 15 240, Shipper Best By Code: Aug 28, 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:
CSM Bakery Products NA
Reason for Recall:
Foreign matter (rigid plastic pieces) found in peanut butter bars.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Daily Chef Peanut Butter Bars, Net Wt. 27 oz (1 lb 11 oz) 765g, Made in Canada, Manufactured for: CSM Bakery Products NA, Inc., Tucker, GA 30084

Product Codes/Lot Numbers:

UPC Code: 78742 11172, Lot: TFF 15 237, Shipper Best By Code: Aug 25, 2016; Lot: TFF 15 238, Shipper Best By Code: Aug 26, 2016; Lot: TFF 15 239, Shipper Best By Code: Aug 27, 2016, Lot: TFF 15 226, Shipper Best By Code: Aug 14, 2016; Lot: TFF 15 240, Shipper Best By Code: Aug 28, 2016.

Distribution:

Distributed in: CA, FL, GA, IL, IN, LA, MO, NC, NY, PA, OH, OK, TX, WI, WY

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0323-2016

Related Recalls