Vinyard Fruit & Vegetable Recalls 7109 Veg Kit for Listeria Risk
Vinyard Fruit & Vegetable Co., Inc. is recalling 7109 Veg Kit products due to potential contamination with Listeria monocytogenes.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. 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
Vinyard Fruit & Vegetable Co., Inc. is recalling 1,066 cases of 7109 Veg Kit, (Broc, Caul, Carr, Cele) 4/3# packaged in plastic flexible bags. The recall is being conducted because the product has the potential to be contaminated with Listeria monocytogenes.
The affected product is identified by codes 277 through 306. The recall covers distribution in Oklahoma (OK) and Arkansas (AR).
Consumers who have purchased this product should check their inventory for the specific codes listed above. If the product is found, it should be discarded or returned to the place of purchase.
The recalled product
- Product
- 7109 Veg Kit, (Broc, Caul, Carr, Cele) 4/3# packaged in plastic flexible bags
- Manufacturer
- Vinyard Fruit & Vegetable Co., Inc.
- Category
- Food — Vegetables
- Hazard
- Affected units
- 1,066
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 (1)
- 277 thru 306
Distribution
Part of a larger recall action
This product is one of 7 recalled by Vinyard Fruit & Vegetable Co., Inc. 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.
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