Keurig Dr Pepper recalls Target Good & Gather Coconut Pineapple Sparkling Water and 3 more: allergen risk
Find the official FDA enforcement report
Recall at a glance
- Recalling company
- Keurig Dr Pepper
- Location
- Frisco, TX
- Reported by FDA
- December 8, 2021
- Recall started
- October 14, 2021
- Risk class
- Class II
- Status (latest data we have)
- Terminated
- Type
- Voluntary: Firm initiated
- Category
- Beverages
- Reason type
- Undeclared allergensLabeling and quality
Is my product affected?
Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.
- Target Good & Gather Coconut Pineapple Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 04059 1, UPC outer carton (8 pack): 0 85239 03833 8
Quantity: 2,148 cases
Codes: Date codes: BestBy30JULY2022 - 7UP Zero Sugar Lemon Lime Soda 12 pack of 12 oz. can UPC Cardboard Wrap Code: 7800001181 UPC Can Code: 0780790
Quantity: 9152 cases
Codes: Product Code Date: H1217 CB3W - Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110
Quantity: 7,849 cases
Codes: Product Code Date: 12/16/2022 KDC - Target Good & Gather Mixed Berry Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 11516 9, UPC outer Carton (8 pack): 0 85239 11345 5
Quantity: 9,393 cases
Codes: Date codes: BestBy18JUNE2022
Where it was distributed
Nationwide
What to do
If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.
Frequently asked questions
What was recalled?
Keurig Dr Pepper recalled 4 products, including Target Good & Gather Coconut Pineapple Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 04059 1, UPC outer carton (8 pack): 0 85239….
Why was it recalled?
The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained unlabeled sulfites.
What does Class II mean?
FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Where was it sold or shipped?
Nationwide
What should I do if I have this product?
Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.
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Sources
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