CLASS I Food recall · Reported 17 Feb 2021 · FDA Enforcement Report

Sprout's Vanilla Flavored Yogurt Covered Cranberries recalled

Ohio Hickory Harvest Brand Products is recalling Sprout's Vanilla Flavored Yogurt Covered Cranberries, distributed in Texas. The recall was initiated on 2 Feb 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC Code 646670463778 Batch No. 20149 (RR) Best By 05/28/21 Product No. 320059
Quantity recalled409 Cases - 4908 individual units

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-0279-2021
FDA event ID
87275
Recalling firm
Ohio Hickory Harvest Brand Products, Akron, OH
Classification
Class I
Status
Terminated
Recall initiated
2 Feb 2021
FDA classified
10 Feb 2021
Reported
17 Feb 2021
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Tree Nuts
Product category
Yogurt

Timeline

2 Feb 2021Recall initiated by company
10 Feb 2021Classified by FDA+8 days
17 Feb 2021Published 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

Undeclared Allergen of Tree Nuts : Almonds

Product as listed by the FDA

Sprout's Vanilla Flavored Yogurt Covered Cranberries UPC 646670463778 12 Ounce Stand-Up Pouch Bag Ambient Storage

Where it was distributed

All product delivered to a single distribution center in Flower Mound, TX.

Texas

Questions about this recall

Why was it recalled?

Undeclared Allergen of Tree Nuts : Almonds

Which lots are affected?

UPC Code 646670463778 Batch No. 20149 (RR) Best By 05/28/21 Product No. 320059

Where was it sold?

All product delivered to a single distribution center in Flower Mound, TX.

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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