RecallHawk
Class II Recall

1. Sqwincher Electrolyte Beverage Mix, orange powder packs, Net Wt 23.83 oz (1 lb 8 oz) 675.6 g: UPC 7588025004; package

Kent Precision Foods Group, Inc.

Summary

The FDA issued a Class II for 1. Sqwincher Electrolyte Beverage Mix, orange powder packs, Net Wt 23.83 oz (1 l by Kent Precision Foods Group, Inc.. Reason: Potential foreign material (metal).

Details

Source

Food Recall

External ID

F-0007-2025

Action Date

2024-10-09

Status

Terminated

Category

food

Product Description

1. Sqwincher Electrolyte Beverage Mix, orange powder packs, Net Wt 23.83 oz (1 lb 8 oz) 675.6 g: UPC 7588025004; packaged in assorted case, 32 per case / 2.5 gal yield item number 159016044 2. Sqwincher Electrolyte Beverage Mix, grape powder packs, Net Wt 23.83 oz (1 lb 8 oz) 675.6 g: UPC 7588025007; packaged in assorted case, 32 per case / 2.5 gal yield item number 159016044 3.Sqwincher Electrolyte Beverage Mix, lemon-lime powder packs, Net Wt 23.83 oz (1 lb 8 oz) 675.6 g: UPC 7588025002; packaged in assorted case, 32 per case / 2.5 gal yield item number 159016044 4.Sqwincher Electrolyte Beverage Mix, fruit punch powder packs, Net Wt 23.83 oz (1 lb 8 oz) 675.6 g: UPC 7588025001; packaged in assorted case, 32 per case / 2.5 gal yield item number 159016044

Lot/Code Info: lot# 2B0158245 Best By: 4/26/2026

Quantity Affected: 1231 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

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-0007-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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