FDA recall record

ConAgra Foods Watts Brothers Farms Organic Mixed Vegetables, UPC recall — FDA F-2278-2016

Organic Mixed Vegetables are recalled due to the potential to be contaminated with Listeria monocytogenes.

Class Iclassification
F-2278-2016official record ID
Sep 21, 2016report date

Recall record at a glance

Official recordF-2278-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmConAgra Foods Inc.
Report dateSep 21, 2016
Recall initiation dateMay 5, 2016
Quantity7,543,480 lbs. - expanded recall 2,962,179 lbs.
LocationOmaha, NE, United States

Official product description

Watts Brothers Farms Organic Mixed Vegetables, UPC 681241053484. ************Foodservice Products******************** Watts Tote 4-Way Mixed Vegetables, item 3902 Watts Brothers 5 Way Mixed Vegetables, item V5173 Watts Brothers 4 Way Mixed Vegetables, item V5218 Watts Brothers 5 Way Mixed Vegetables, item V5246 Watts Brothers 4 Way Mixed Vegetables, item V5412 Sc 3623 12/40 oz 5-Way Mixed Vegetables, item V5359 Sc 2975 1/30# 5-Way Mixed Vegetables, item V5363 Sr 4493 12/40 oz 5-Way Mixed Vegetables, item V5370 Sr 2991 1/30# 5-Way Mixed Vegetables, item V5374 Alasko 6/2Kg 4-Way Mixed Vegetables, item V5448 Alasko 6/2Kg 4-Way Mixed Vegetables, item V5453 *********NICHIREI BRANDS ARE NOT DISTRIBUTED IN THE US***** Nichirei Organic Mixed Vegetables, item V5600, UPC 4 902130 363641. Nichirei Value + Organic Mixed Vegetables, item V5803, UPC 4 949486 327019

Why the product was recalled

Organic Mixed Vegetables are recalled due to the potential to be contaminated with Listeria monocytogenes.

Distribution information

distributed in AZ, CA, CO, FL, HI, IA, ID, IL, LA, MD, MN, NJ, NV, OH, OK, PA, TX, UT, VA, and WI and in the following countries: Canada, Columbia, Japan, and Panama.

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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