The Recall Desk
SevereFDA (Food)·F-1775-2016·Announced 2016-08-03

CRF Frozen Foods Recalls Supreme Bean & Carrot Blend for Listeria Risk

CRF Frozen Foods is recalling VIP brand Supreme Bean & Carrot Blend due to potential Listeria monocytogenes contamination. The product was distributed in the US, Canada, and Japan.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class I, which mandates a minimum severity score of 4 according to the rubric.

Plain-English summary

CRF Frozen Foods, LLC is recalling VIP brand Supreme Bean & Carrot Blend, a frozen product with a net weight of 14 ounces. The recall is issued because the product has the potential to be contaminated with Listeria monocytogenes. The ingredient statement for the product declares only Beans and Carrots.

The affected product has a UPC of 7007705002. All affected units have best by or sell by dates between April 26, 2016, and April 26, 2018. The product code format is 3756 107 16 08:27 A USA/CANADA. The total quantity involved in the recall is 19,8923 lbs.

The product was distributed nationwide in the United States, as well as in Canada and Japan. Consumers should check their pantries for this specific product and dispose of it or return it to the place of purchase if they have it.

The recalled product

Product
Supreme Bean & Carrot Blend, brand VIP, frozen, net wt. 14oz. UPC 7007705002 The ingredient statement declares: Beans and Carrots.
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • All affected products have the best by dates or sell by dates between April 26
  • 2016 and April 26

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 27 recalled by CRF Frozen Foods, LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 27 products in this recall →