CLASS II Food recall · Reported 8 Dec 2021 · FDA Enforcement Report

Target Good & Gather Coconut Pineapple Sparkling Water recalled

Keurig DR Pepper is recalling Target Good & Gather Coconut Pineapple Sparkling Water, distributed nationwide in the US. The recall was initiated on 14 Oct 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesDate codes: BestBy30JULY2022
Quantity recalled2,148 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0241-2022
FDA event ID
88931
Recalling firm
Keurig DR Pepper, Frisco, TX
Classification
Class II
Status
Terminated
Recall initiated
14 Oct 2021
FDA classified
2 Dec 2021
Reported
8 Dec 2021
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sulfites
Product category
Soda

Timeline

14 Oct 2021Recall initiated by company
2 Dec 2021Classified by FDA+49 days
8 Dec 2021Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Product as listed by the FDA

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

Where it was distributed

Nationwide

Nationwide

Stores named: Target

Questions about this recall

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.

Which lots are affected?

Date codes: BestBy30JULY2022

Where was it sold?

Nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 88931

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