Polar Black Cherry Premium Seltzer recalled for unlabeled sulfites
Keurig Dr Pepper is recalling Polar Black Cherry Premium Seltzer 12-packs due to unlabeled sulfites. The recall affects 7,849 cases distributed nationwide with product code date 12/16/2022.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II recall involving allergen mislabeling (unlabeled sulfites). Sulfites are a known allergen that can trigger serious reactions in sensitive individuals. No illnesses or injuries have been reported in the source text, but the hazard poses a direct risk of harm to affected consumers.
Plain-English summary
Keurig Dr Pepper is recalling Polar Black Cherry Premium Seltzer 12-pack of 12oz cans (UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110) due to the presence of unlabeled sulfites. The company received complaints of off flavor and off aroma, and analysis identified unlabeled sulfites in the affected products.
The recall applies to 7,849 cases distributed nationwide. The affected product has a code date of 12/16/2022 KDC.
Consumers who have purchased this product should stop consuming it if they are sensitive or allergic to sulfites. Persons with sulfite sensitivity may experience allergic reactions. Consumers should contact Keurig Dr Pepper with questions or concerns regarding this recall.
The recalled product
- Product
- Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110
- Manufacturer
- KEURIG DR PEPPER
- Category
- Food — Beverages / Seltzer
- Affected units
- 7,849
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Product Code Date: 12/16/2022 KDC
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 recalled by KEURIG DR PEPPER under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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