Sqwincher Electrolyte Beverage Mix, Orange powder pack, Net Wt 47.66 oz (3lb) 1.35 kg: UPC 7588008834 / 16 per case / 5
Summary
The FDA issued a Class II for Sqwincher Electrolyte Beverage Mix, Orange powder pack, Net Wt 47.66 oz (3lb) 1. by Kent Precision Foods Group, Inc.. Reason: Potential foreign material (metal).
Details
Source
Food Recall
External ID
F-0006-2025
Action Date
2024-10-09
Status
Terminated
Category
food
Product Description
Sqwincher Electrolyte Beverage Mix, Orange powder pack, Net Wt 47.66 oz (3lb) 1.35 kg: UPC 7588008834 / 16 per case / 5 gal yield item number 159016404
Lot/Code Info: lot# 2B0165712 Best By: 4/25/2026
Quantity Affected: 251 cases
Reason for Recall
Potential foreign material (metal)
Distribution
AL, ID, IL, MN, MO, NC, NY, OH, PA, TN, and WI
Type: Voluntary: Firm initiated
Recall Initiated: 2024-09-09
Company
Muscatine, IA
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 38 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Kent Precision Foods Group, Inc. 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 (Kent Precision Foods Group, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kent Precision Foods Group, Inc. have FDA actions?
Kent Precision Foods Group, Inc. 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-0006-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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