FDA recall record

Kent Precision Foods Group Sqwincher Electrolyte Beverage Mix, Orange powder pack, Net Wt recall — FDA F-0006-2025

Potential foreign material (metal)

Class IIclassification
F-0006-2025official record ID
Oct 9, 2024report date

Recall record at a glance

Official recordF-0006-2025
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKent Precision Foods Group, Inc.
Report dateOct 9, 2024
Recall initiation dateSep 9, 2024
Quantity251 cases
LocationMuscatine, IA, United States

Official 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

Why the product was recalled

Potential foreign material (metal)

Distribution information

AL, ID, IL, MN, MO, NC, NY, OH, PA, TN, and WI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.