CLASS I Food recall · Reported 8 Jul 2020 · FDA Enforcement Report

Hill Country Fare Citrus Punch Drink CONT recalled by He Butt

He Butt is recalling Hill Country Fare Citrus Punch Drink CONT, distributed in Texas. The recall was initiated on 16 Jun 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes9/30/2020 and 10/1/2020
Quantity recalled29,132 bottles

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-1008-2020
FDA event ID
85892
Recalling firm
He Butt, San Antonio, TX
Classification
Class I
Status
Terminated
Recall initiated
16 Jun 2020
FDA classified
1 Jul 2020
Reported
8 Jul 2020
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Juice

Timeline

16 Jun 2020Recall initiated by company
1 Jul 2020Classified by FDA+15 days
8 Jul 2020Published in enforcement report+7 days

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

Reason for recall

Potential to contain undeclared milk

Product as listed by the FDA

Hill Country Fare Citrus Punch Drink 1 GAL CONT. NET. 3.78L Contains 0% Juice UPC 4122081863

Where it was distributed

Retail stores throughout Texas

Texas

Stores named: H-E-B

Questions about this recall

Why was it recalled?

Potential to contain undeclared milk

Which lots are affected?

9/30/2020 and 10/1/2020

Where was it sold?

Retail stores throughout Texas

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.

Other products in this recall event

3 other products · FDA event 85892

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