Food recall

Peak Cocktails recall: Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12

Peak Cocktails, of Columbus, OH, recalled Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12. The FDA's reason: “Overpressurization leading to exploding cans.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on June 3, 2025, and the FDA first listed it in its Enforcement Report of July 9, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Other germs or toxins (botulism, hepatitis A, mold...)

Status

Terminated

Closed February 17, 2026

The recall

Company
Peak Cocktails (Columbus, OH)
Reason, in FDA's words
“Overpressurization leading to exploding cans”
Where it was sold
Product was distributed to consumers in: AK, AL, AR, AZ, CA, CO, CT, District of Columbia, DE, FL, GA, HI, 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, and WY.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
97024

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0203-2025 Class II

    Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24, and 48 cans. Batch Codes: B25127, B25128; Packaging Date: 05/07/2025, 05/08/2025

    Codes: UPC: 860013380571; Batch Codes: B25127, B25128; Packaging Dates: 05/07/2025, 05/08/2025

    Quantity: 16,128 units

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 9, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.