SunGlow Unsalted Margarine (Ventura Foods) – Undeclared Soy (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
SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC 26700-13499. Outer case: Net Wt 36 lb (16.32 kg). UPC 1 00 26700 13499 6. Ventura Foods, Brea, CA 92821
Brand
Ventura Foods Llc
Lot Codes / Batch Numbers
Lot Codes: MMAY0818 and 05.08.18, MMAY1518 and 05.15.18, MMAY2118 and 05.21.18, MMAY2918 and 05.29.18, MJUN0518 and 06.05.18, MJUN1218 and 06.12.18, MJUN1918 and 06.19.18, MJUN2618 and 06.26.18
Products Sold
Lot Codes: MMAY0818 and 05.08.18, MMAY1518 and 05.15.18, MMAY2118 and 05.21.18, MMAY2918 and 05.29.18, MJUN0518 and 06.05.18, MJUN1218 and 06.12.18, MJUN1918 and 06.19.18, MJUN2618 and 06.26.18
Ventura Foods Llc is recalling SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Kee due to SunGlow contains undeclared soy lecithin.. 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
SunGlow contains undeclared soy lecithin.
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
AL, AK, AR, CO, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MI, MN, MS, MO, MT, NE, NV, NJ, NM, NY, ND, OH, OK, OR, PA, SC, SD, TX, VT, WA, WI
Page updated: Jan 6, 2026