Hamburger buns, 4.5" in unlabeled clear plastic bags, 30 or 12 buns per bag.
Summary
The FDA issued a Class II for Hamburger buns, 4.5" in unlabeled clear plastic bags, 30 or 12 buns per bag. by Kansas City LLC., DBA Best Harvest Bakeries. Reason: Positive environmental samples analyzed for Listeria and Salmonella species..
Details
Source
Food Recall
External ID
F-0081-2022
Action Date
2021-11-10
Status
Terminated
Category
food
Product Description
Hamburger buns, 4.5" in unlabeled clear plastic bags, 30 or 12 buns per bag.
Lot/Code Info: 2-feb-22
Quantity Affected: 10,712 buns total
Reason for Recall
Positive environmental samples analyzed for Listeria and Salmonella species.
Distribution
Distributed to restaurants in AR, CO, IA, KS, LA, MN, MO, ND, NE, NM OK, SD, TX, WI, and WY
Type: Voluntary: Firm initiated
Recall Initiated: 2021-08-13
Company
Kansas City, KS
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 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Kansas City LLC., DBA Best Harvest Bakeries has 7 FDA actions in our database, including 7 recalls.
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 (Kansas City LLC., DBA Best Harvest Bakeries) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kansas City LLC., DBA Best Harvest Bakeries have FDA actions?
Kansas City LLC., DBA Best Harvest Bakeries has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0081-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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