Peak Cocktails Blood Orange Spritz recall
Recalled by Peak Cocktails · Columbus, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Overpressurization leading to exploding cans
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
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
Quantity: 16,128 units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
UPC: 860013380571; Batch Codes: B25127, B25128; Packaging Dates: 05/07/2025, 05/08/2025
Where it was sold
Alaska Alabama Arkansas Arizona California Colorado Connecticut District of Columbia Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin Wyoming
FDA's distribution note: 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.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Peak Cocktails
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 3, 2025
- In FDA report of
- Jul 9, 2025
- Terminated
- Feb 17, 2026
- FDA recall number
- H-0203-2025 · event 97024
- Official record
- FDA enforcement report search