FDA recall record

Taher Fresh Seasons, Fresh Veggie & Ranch Cup, 7.5 ounces, packaged recall — FDA F-0345-2020

The Fresh Seasons, Fresh Veggie & Ranch Cup is being recalled because it contains cauliflower that was recalled by Mann Packing Co., Inc. because it has…

Class Iclassification
F-0345-2020official record ID
Dec 4, 2019report date

Recall record at a glance

Official recordF-0345-2020
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmTaher, Inc.
Report dateDec 4, 2019
Recall initiation dateNov 4, 2019
Quantity56 individual units
LocationPlymouth, MN, United States

Official product description

Fresh Seasons, Fresh Veggie & Ranch Cup, 7.5 ounces, packaged in a plastic 12 ounce cup

Why the product was recalled

The Fresh Seasons, Fresh Veggie & Ranch Cup is being recalled because it contains cauliflower that was recalled by Mann Packing Co., Inc. because it has the potential to be contaminated with Listeria monocytogenes. This recall is connected to a voluntary recall of vegetable products announced by Mann Packing Co., Inc. on November 3 after they were notified by the Food and Drug Administration and the Canadian Food Inspection Agency of potential contamination.

Distribution information

The firm placed this product in their firm-owned workplace vending machines, and further distributed the products to 1 consignee who also placed this product in workplace vending machines

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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