Imperial Thickened Cranberry Cocktail Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 carto
Summary
The FDA issued a Class II for Imperial Thickened Cranberry Cocktail Nectar packaged in combi-bloc multi wall by Lyons Magnus LLC. Reason: Indication of product spoilage.
Details
Source
Food Recall
External ID
F-0060-2023
Action Date
2022-10-26
Status
Terminated
Category
food
Product Description
Imperial Thickened Cranberry Cocktail Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Lot/Code Info: Batch/Lot No. 1422, 2422, 3422, 4422 Product No. 5256, 1711, 1773, 3301, 1771, 5258, 3302, 1787, 1774, 3304, 3305, 1785 Best By: 03/27/23, 03/28/23, 03/29/23, 03/30/23
Quantity Affected: 2094 cases
Reason for Recall
Indication of product spoilage
Distribution
AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV
Type: Voluntary: Firm initiated
Recall Initiated: 2022-09-23
Company
Fresno, CA
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 41 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lyons Magnus LLC has 26 FDA actions in our database, including 26 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 (Lyons Magnus LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lyons Magnus LLC have FDA actions?
Lyons Magnus LLC has 26 FDA actions in our database, including 26 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0060-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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