RecallHawk
Class I Recall

Sprouts Farmers Market Dark Chocolate Covered Cherries; Dried Cherries covered in Rich Dark Chocolate. Net Wt. 12 oz

Torn & Glasser, Inc.

Summary

The FDA issued a Class I for Sprouts Farmers Market Dark Chocolate Covered Cherries; Dried Cherries covered by Torn & Glasser, Inc.. Reason: Packaged of Dark Chococlate Covered Cherries may contain Dark Chocolate covered almonds. Undeclared allergen - tree nuts (almonds)..

Details

Source

Food Recall

External ID

F-0907-2022

Action Date

2022-03-30

Status

Terminated

Category

food

Product Description

Sprouts Farmers Market Dark Chocolate Covered Cherries; Dried Cherries covered in Rich Dark Chocolate. Net Wt. 12 oz (340g) Item # 638-011 UPC: 6 46670 46342 6 Processed in a facility that processes on shared equipment with peanuts, tree nuts, wheat and milk. Distributed by Sprouts Farmers Market, Phoenix, AZ

Lot/Code Info: Case Lot # 795935; Bag Lot # 3001 A Sell by Date: 7/24/2022

Quantity Affected: 231 cases (2,772 Units)

Reason for Recall

Packaged of Dark Chococlate Covered Cherries may contain Dark Chocolate covered almonds. Undeclared allergen - tree nuts (almonds).

Distribution

Arizona, California, Colorado, Nevada, New Mexico, and Utah.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-03-03

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 52 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Torn & Glasser, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Torn & Glasser, Inc. have FDA actions?

This is the only FDA action we have on record for Torn & Glasser, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0907-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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