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Class IITerminated in FDA datasetRecall initiated Jun 3, 2025

Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in…

Recalling firm: Peak Cocktails

Why it was recalled

Overpressurization leading to exploding cans

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 17, 2026.

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Compare the exact product and package details with the label you have.

ProductPeak 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
Package size8.4 fl oz
UPC860013380571

FDA code information

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

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC860013380571UPC: 860013380571; Batch Codes: B25127, B25128; Packaging Dates: 05/07/2025, 05/08/2025
batchB25127UPC: 860013380571; Batch Codes: B25127, B25128; Packaging Dates: 05/07/2025, 05/08/2025
batchB25127an individual flavor and in variety packs of 12, 24, and 48 cans. Batch Codes: B25127, B25128; Packaging Date: 05/07/2025, 05/08/2025
batchB25128UPC: 860013380571; Batch Codes: B25127, B25128; Packaging Dates: 05/07/2025, 05/08/2025
batchB25128idual flavor and in variety packs of 12, 24, and 48 cans. Batch Codes: B25127, B25128; Packaging Date: 05/07/2025, 05/08/2025

Original FDA recall reason

Overpressurization leading to exploding cans

Recall details

Recall number
H-0203-2025
Event ID
97024
FDA status
Terminated
Initiated
Jun 3, 2025
Reported
Jul 9, 2025
Classified
Jun 27, 2025
Terminated
Feb 17, 2026
Quantity
16,128 units
Location
Columbus, OH, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

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.

FDA source record · H-0203-2025

Data updated September 16, 2026. View official FDA data ↗

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