RecallHawk
Class II Recall

Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,

Peak Cocktails

Summary

The FDA issued a Class II for Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual by Peak Cocktails. Reason: Overpressurization leading to exploding cans.

Details

Source

Food Recall

External ID

H-0203-2025

Action Date

2025-07-09

Status

Terminated

Category

food

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

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

Quantity Affected: 16,128 units

Reason for Recall

Overpressurization leading to exploding cans

Distribution

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.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-06-03

Company

Peak Cocktails

Columbus, OH

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 154 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (Peak Cocktails) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Peak Cocktails have FDA actions?

This is the only FDA action we have on record for Peak Cocktails in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0203-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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