CLASS I Food recall · Reported 15 Nov 2023 · FDA Enforcement Report

Kula Can Pin¿a Colada + Kratom Seltzer Dietary Supplement recalled

Kula Brands is recalling Kula Can Pin¿a Colada + Kratom Seltzer Dietary Supplement. The recall was initiated on 21 Sep 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot Number U17831532PNCL Exp. Date 7/27/24
Quantity recalled7,062 cans

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-0320-2024
FDA event ID
93157
Recalling firm
Kula Brands, Naples, FL
Brand
Kula
Classification
Class I
Status
Terminated
Recall initiated
21 Sep 2023
FDA classified
3 Nov 2023
Reported
15 Nov 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Allergens
Product category
Soda

Timeline

21 Sep 2023Recall initiated by company
3 Nov 2023Classified by FDA+43 days
15 Nov 2023Published in enforcement report+12 days

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

Reason for recall

Undeclared Allergens: Milk and Tree Nut (Coconut) and Unapproved Food Additive: Kratom

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Kula Can Pin¿a Colada + KRATOM SELTZER, 12 oz (355ML) DIETARY SUPPLEMENT

Where it was distributed

Domestic distribution only.

Questions about this recall

Why was it recalled?

Undeclared Allergens: Milk and Tree Nut (Coconut) and Unapproved Food Additive: Kratom

Which lots are affected?

Lot Number U17831532PNCL Exp. Date 7/27/24

Where was it sold?

Domestic distribution only.

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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.

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