House Blend Barbecue Sauce (Diamond Crystal) – Incorrect Label (2018)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
HOUSE BLEND Barbecue SAUCE INGREDIENTS: ***Contains 2% or less of Soybean Oil***Onion Powder***Calcium Disodium EDTA***DIAMOND CRYSTAL BRANDS, INC. SAVANNAH, GA 31405
Brand
Diamond Crystal Brands, Inc.
Lot Codes / Batch 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)
Products Sold
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)
Diamond Crystal Brands, Inc. is recalling HOUSE BLEND Barbecue SAUCE INGREDIENTS: ***Contains 2% or less of Soybean Oil***Onion Powder***Calci due to During a label check the firm noticed that the product was shipped with the incorrect label. The label is missing the following ingredients: Soybean O. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, GA, IL, LA, MA, MI, NJ, NC, OH, PA, TN
Page updated: Jan 6, 2026