Rococo Ice Cream 15% base mix; list Kingdom Creamery of Vermont on the product label
Summary
The FDA issued a Class I for Rococo Ice Cream 15% base mix; list Kingdom Creamery of Vermont on the product l by Kingdom Creamery of Vermont LLC. Reason: Product may be contaminated Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1597-2022
Action Date
2022-08-24
Status
Terminated
Category
food
Product Description
Rococo Ice Cream 15% base mix; list Kingdom Creamery of Vermont on the product label
Lot/Code Info: Best By Date: 8/14/22 Lot: 220727
Quantity Affected: 1,623 cases (total all products)
Reason for Recall
Product may be contaminated Listeria monocytogenes.
Distribution
VT, ME, MA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-07-29
Company
East Hardwick, VT
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 38 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Kingdom Creamery of Vermont LLC has 14 FDA actions in our database, including 14 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Kingdom Creamery of Vermont LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kingdom Creamery of Vermont LLC have FDA actions?
Kingdom Creamery of Vermont LLC has 14 FDA actions in our database, including 14 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1597-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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