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.
Take action
Contact the company
📍Recalling firmKEURIG DR PEPPER6425 Hall Of Fame Lane, 8th Floor - Kdp Secure Storage · Frisco, TX 75034
✎ GovInfoNow plain-language explainer
Keurig Dr Pepper has recalled Target Good & Gather Coconut Pineapple Sparkling Water because it contains unlabeled sulfites. This matters because people with sulfite allergies may experience adverse reactions without knowing the ingredient is present. The product was sold in 8-packs of 12 oz cans. Read more at govinfonow.com/recall/14004-good-gather-coconut-pineapple-sparkling-water-recall-unlabeled-sulfites.
“Good & Gather Coconut Pineapple Sparkling Water Recall: Unlabeled Sulfites.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/14004-good-gather-coconut-pineapple-sparkling-water-recall-unlabeled-sulfites. Based on FDA recall #F-0241-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0241-2022%22&limit=1).
The FDA announced on 2021-10-14 that Keurig Dr Pepper is recalling Target Good & Gather Coconut Pineapple Sparkling Water because it contains unlabeled sulfites. The recall covers 2,148 cases distributed nationwide.
How to tell if you have it
Brand: Good & Gather
Product: Coconut Pineapple Sparkling Water
Packaging: 8 pack of 12 oz. cans
UPC can: 0 85239 04059 1
UPC outer carton (8 pack): 0 85239 03833 8
Date codes: BestBy30JULY2022
Quantity: 2,148 cases
The hazard
The company received off flavor and off aroma complaints for the recalled lot. Analysis found that the products contained unlabeled sulfites.
Context
GovInfoNow's records show Keurig Dr Pepper has had three other recalls since 2021-09-13, including a 2023-02-03 Celestial Seasonings Tea Recall for undeclared caffeine and a 2021-12-09 Diet Snapple Tea Peach Tea recall for potential sugar content. Other recent recalls of similar products include Elegant Foods Coconut Flakes Recall (2026-07-24) and Loard's Sea Salt Caramel Ice Cream Recall (2026-04-15).
How to tell if you have this one
Check your cans for the UPC code 0 85239 04059 1 on the can and 0 85239 03833 8 on the outer carton. Verify the date code reads BestBy30JULY2022. The product is an 8 pack of 12 oz cans.
Brand
Good & Gather
Category
Food
FDA recall event · 4 products
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
Nationwide
Recall number
Product, codes & lots
Quantity
F-0239-2022
7UP Zero Sugar Lemon Lime Soda 12 pack of 12 oz. can UPC Cardboard Wrap Code: 7800001181 UPC Can Code: 0780790; Product Code Date: H1217 CB3W
9152 cases
F-0240-2022
Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110; Product Code Date: 12/16/2022 KDC
7,849 cases
F-0241-2022
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; Date codes: BestBy30JULY2022
2,148 cases
F-0242-2022
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; Date codes: BestBy18JUNE2022
9,393 cases
Based on the official FDA remedy
What to do — step by step
Check your product
Verify if your can has UPC 0 85239 04059 1 and the BestBy30JULY2022 date code.
Avoid consumption
Do not consume the product if you have a sulfite allergy due to the unlabeled ingredient.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #F-0241-2022 (October 14, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0241-2022 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.