Golden Gloss 21837. Item# 20658861 / 30728137.LM2 Ingredients: Water, vegetable protein (pea) and less than 2% of dex
Summary
The FDA issued a Class I for Golden Gloss 21837. Item# 20658861 / 30728137.LM2 Ingredients: Water, vegetab by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..
Details
Source
Food Recall
External ID
F-1638-2022
Action Date
2022-09-07
Status
Terminated
Category
food
Product Description
Golden Gloss 21837. Item# 20658861 / 30728137.LM2 Ingredients: Water, vegetable protein (pea) and less than 2% of dextrose, maltodextrin, sunflower oil. Net Wt. 34.06 lb (15.45G) Distributed by Kerry Beloit, WI 53511
Lot/Code Info: Lot Code 3902 / Best By Date 12/29/2022; Lot Code 4902 / Best By Date 12/30/2022. EXPANDED 08-10-2022 Lot Code 4402 / Best By Date 11/10/2022 Lot Code 5402 / Best By Date 11/11/2022
Quantity Affected: 53,818,025 total units
Reason for Recall
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2022-07-22
Company
Fresno, CA
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 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lyons Magnus, Inc has 78 FDA actions in our database, including 78 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 (Lyons Magnus, Inc) 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, Inc have FDA actions?
Lyons Magnus, Inc has 78 FDA actions in our database, including 78 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1638-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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