Frozen Peas & Carrots (Lakeside) – 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 Peas & Carrots, Product is IQF, frozen, not ready to eat, each label carries cooking instructions. Product is packaged under the following brand names and sizes: 1. Bountiful Harvest, Net Wt.40 oz. (2.5 lbs.) 1.13 kg, UPC 22486-11902; 2. Giant Eagle, Net Wt 16 oz (1 lb) 454 g, UPC 30034-00993; 3. Our Family, Net Wt 16 oz (454 g), UPC 70253-10513; 4. Sysco Classic, Net Wt 40 oz (2.5 lbs) 1.13 kg, UPC 74865-07850.
Brand
Lakeside Foods, Inc
Lot Codes / Batch Numbers
Bountiful Harvest: Packaging Code: PL25132 / Production Code: 1086893, Giant Eagle: Packaging Code: PL25125 / Production Code: 1086893 Best By 05/2014, Our Family: Packaging Code: PL35132 or PL45132 / Production Code: 1086893, Best By 05/2017 Sysco Classic: Packaging Code: PL25148 / Production Code: PLMB4305, Best By 05/2017
Products Sold
Bountiful Harvest: Packaging Code: PL25132 / Production Code: 1086893; Giant Eagle: Packaging Code: PL25125 / Production Code: 1086893 Best By 05/2014; Our Family: Packaging Code: PL35132 or PL45132 / Production Code: 1086893, Best By 05/2017 Sysco Classic: Packaging Code: PL25148 / Production Code: PLMB4305, Best By 05/2017
Lakeside Foods, Inc is recalling Frozen Peas & Carrots, Product is IQF, frozen, not ready to eat, each label carries cooking instruct due to The Ohio Department of Agriculture conducted testing on the product and found it positive for Listeria monocytogenes.. 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
The Ohio Department of Agriculture conducted testing on the product and found it positive for Listeria monocytogenes.
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
IA, MN, MO, NE, ND, OH, WI
Page updated: Jan 6, 2026