Charles Boggini Company Cola Flavoring Base; packaged in 1 gallon jugs and 5 gallon pails
Summary
The FDA issued a Class II for Charles Boggini Company Cola Flavoring Base; packaged in 1 gallon jugs and 5 gal by Charles Boggini Company Llc. Reason: Products contain undeclared sulfites..
Details
Source
Food Recall
External ID
F-1285-2024
Action Date
2024-06-12
Status
Terminated
Category
food
Product Description
Charles Boggini Company Cola Flavoring Base; packaged in 1 gallon jugs and 5 gallon pails
Lot/Code Info: Lot/Unit Numbers: 9-330, 9-348, 1-013, 1-036, 1-097
Quantity Affected: 2723 gallons
Reason for Recall
Products contain undeclared sulfites.
Distribution
CT, PA, NY, NJ, AZ, MI, IL, NV, CA
Type: Voluntary: Firm initiated
Recall Initiated: 2024-03-29
Company
Coventry, CT
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 77 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Charles Boggini Company Llc has 3 FDA actions in our database, including 3 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 (Charles Boggini Company Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Charles Boggini Company Llc have FDA actions?
Charles Boggini Company Llc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1285-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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