Wylwood Frozen Corn (Bonduelle) – Listeria Contamination (2015)
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
Frozen Corn distributed under the following labels and sizes: (a) WYLWOOD Super Sweet Whole Kernel Corn, NET WT. 16 OZ (1 LB), UPC 051933002401, DISTR. BY: SAVE-A-LOT FOOD STORES LTD. EARTH CITY, MO 63045; (b) MARKET BASKET Cut Corn, NET WT. 16 OZ. (1 LB.), UPC 049705693414, Packed Exclusively for: DEMOULAS SUPERMARKETS, INC. Tewksbury, MA 01876; (c) Bountiful Harvest WHOLE KERNEL CUT CORN, NET WT. 40 OZ. (2.5 LBS.), UPC 822486120597, Marketed by: Independent Marketing Alliance Houston, TX 770
Brand
Bonduelle USA Inc
Lot Codes / Batch Numbers
Codes: (a) Best By June 2017 K51564 and K51574, (b) Best By June 2017 K51574, (c) Best By June 2017 K51574, (d) Best By June 2017 K51574
Products Sold
Codes: (a) Best By June 2017 K51564 and K51574; (b) Best By June 2017 K51574; (c) Best By June 2017 K51574; (d) Best By June 2017 K51574
Bonduelle USA Inc is recalling Frozen Corn distributed under the following labels and sizes: (a) WYLWOOD Super Sweet Whole Kernel C due to One code of Wylwood brand Frozen Whole Kernel Corn was found to be contaminated with Listeria monocytogenes based on sampling and analysis by the Stat. 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
One code of Wylwood brand Frozen Whole Kernel Corn was found to be contaminated with Listeria monocytogenes based on sampling and analysis by the State of Tennessee. The firm decided to recall other labels and codes produced the same day as the suspect lot as a precaution.
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
FL, IN, KY, LA, MD, MA, MS, NJ, NY, NC, OH, PA, VT, VA
Page updated: Jan 6, 2026