CLASS I Food recall · Reported 30 Nov 2016 · FDA Enforcement Report

Stewart's Sportade Fruit Punch Isotonic Beverage recalled

Stewarts Shops is recalling Stewart's Sportade Fruit Punch Isotonic Beverage, distributed in New York, Vermont. The recall was initiated on 26 Oct 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesExpiration date code DEC 02 (found on the neck of the bottle)
Quantity recalled1622 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-0501-2017
FDA event ID
75547
Recalling firm
Stewarts Shops, Saratoga Springs, NY
Classification
Class I
Status
Terminated
Recall initiated
26 Oct 2016
FDA classified
22 Nov 2016
Reported
30 Nov 2016
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Milk
Product category
Other

Timeline

26 Oct 2016Recall initiated by company
22 Nov 2016Classified by FDA+27 days
30 Nov 2016Published in enforcement report+8 days

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

Reason for recall

The specific code of SPORTADE FRUIT PUNCH may contain undeclared milk.

Product as listed by the FDA

Stewart's SPORTADE FRUIT PUNCH Isotonic Beverage 20 Fl Oz (591 mL), UPC 0 82086 31006 8. The product is packaged in a plastic bottle, and has a black label with a red plastic cap.

Where it was distributed

Upstate New York and Southern Vermont

New YorkVermont

Questions about this recall

Why was it recalled?

The specific code of SPORTADE FRUIT PUNCH may contain undeclared milk.

Which lots are affected?

Expiration date code DEC 02 (found on the neck of the bottle)

Where was it sold?

Upstate New York and Southern Vermont

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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