Bob Evan's Sour Cream & Chive Mashed Potatoes 24oz plastic trays with clear film and sleeve over wrap sold as singles t
Summary
The FDA issued a Class II for Bob Evan's Sour Cream & Chive Mashed Potatoes 24oz plastic trays with clear fil by RON DAVIES JR. Reason: Incorrect packaging for product resulting in an undeclared wheat allergen.
Details
Source
Food Recall
External ID
F-0874-2022
Action Date
2022-03-23
Status
Terminated
Category
food
Product Description
Bob Evan's Sour Cream & Chive Mashed Potatoes 24oz plastic trays with clear film and sleeve over wrap sold as singles to consumers
Lot/Code Info: UPC: 07590000524 Line Code Stamp KCL2 Use By 02/28/2022
Quantity Affected: 3354 cases
Reason for Recall
Incorrect packaging for product resulting in an undeclared wheat allergen
Distribution
WI, TN, MA, NY, IA, WV, OH, PA, VA, KY, NJ, MI, IL, IN, MN
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-23
Company
New Albany, OH
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 122 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (RON DAVIES JR) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does RON DAVIES JR have FDA actions?
This is the only FDA action we have on record for RON DAVIES JR in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0874-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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