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FDA recall record

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. B...

Recall F-0158-2016Class IITerminatedAugust 28, 2015

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of March 9, 2016. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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. 40 oz. 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. 13 kg, UPC 74865-07850.

Reason

The Ohio Department of Agriculture conducted testing on the product and found it positive for Listeria monocytogenes.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • 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. 40 oz. 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. 13 kg, UPC 74865-07850.

Code information listed by FDA

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

Distribution and firm information

Recalling firm listed by FDA: Lakeside Foods, Inc

Firm location listed by FDA: Manitowoc, WI, United States

Distribution reported by FDA: US only: IA, MN, MO, ND, NE, OH, WI.

Product quantity listed by FDA: 2677 Cases (12 packages per case)

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.