Urban River Spirits recalls Cafe Caramel Delight non-alcoholic cocktail mixers due to potential under-processing in unlicensed facilities. Consumers should check product labels for the 750ml glass bottle and contact the company for details.
Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
Urban River Spirits is recalling their Cafe Caramel Delight non-alcoholic cocktail mixers because they were made in an unlicensed and uninspected facility, raising safety concerns about under-processing. This recall affects consumers who purchased the product in glass 75:0ml bottles.
The product was made in an unlicensed and uninspected facility, which could lead to under-processing. Under-processing might mean the product isn't safe for consumption, potentially causing health issues.
Anyone who purchased the Cafe Caramel Delight non-alcoholic cocktail mixer from Urban River Spirits. The risk is higher for consumers who use the product for drinking.
Check for the Cafe Caramel Delight label on a glass 750ml bottle. The product was sold under the brand Urban River Spirits.
Look for the Cafe Caramel Delight label on a glass 750ml bottle.
The product was made in an unlicensed and uninspected facility, raising safety concerns about under-processing.
Check for the Cafe Caramel Delight label on a glass 750ml bottle sold under Urban River Spirits.
The recall record does not specify a remedy, so contact Urban River Spirits directly for further instructions.
We’ve drafted a message you can send Urban River Spirits to request your refund or repair — edit it as you like.
Subject: Recall F-1627-2024 — Urban River Spirits Urban River Spirits Hello, I own a Urban River Spirits that is covered by recall F-1627-2024 from Urban River Spirits. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
