🔍 RecallPedia

HOUSE BLEND Barbecue SAUCE INGREDIENTS: ***Contains 2% or less of Soybean Oil***Onion Powder***Calcium Disodium EDTA***DIAMOND CRYSTAL BRANDS, INC. SAVANNAH, GA 31405

Class I - Dangerous
Recalled: October 15, 2018 Diamond Crystal Brands Other Foods

What Should You Do?

  1. Check if you have this product:
    Product still within shelf life (Lot Codes: MH1371J, MH1511J, MK1631J, MH1781J, MI1841J, MI2121J, MH2261J, MI2431J, MH2671J) Product out of shelf life (Lot Codes: MI0111J, MI0301J, MI0441J, MI0491J, MH0571J, MH0661J, MH0831J, MK1021J)
  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:
Diamond Crystal Brands, Inc.
Reason for Recall:
During a label check the firm noticed that the product was shipped with the incorrect label. The label is missing the following ingredients: Soybean Oil, Onion Powder & EDTA.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

HOUSE BLEND Barbecue SAUCE INGREDIENTS: ***Contains 2% or less of Soybean Oil***Onion Powder***Calcium Disodium EDTA***DIAMOND CRYSTAL BRANDS, INC. SAVANNAH, GA 31405

Product Codes/Lot Numbers:

Product still within shelf life (Lot Codes: MH1371J, MH1511J, MK1631J, MH1781J, MI1841J, MI2121J, MH2261J, MI2431J, MH2671J) Product out of shelf life (Lot Codes: MI0111J, MI0301J, MI0441J, MI0491J, MH0571J, MH0661J, MH0831J, MK1021J)

Distribution:

Distributed in: CA, GA, IL, LA, MA, MI, NC, NJ, OH, PA, TN

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0667-2019

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