Heidi's Brownies is packaged in saran wrap in a plastic bag with a twist tie, 3 oz (85g). Label is read in parts: "***H
Summary
The FDA issued a Class III for Heidi's Brownies is packaged in saran wrap in a plastic bag with a twist tie, 3 by Heidi Remington. Reason: Soy Lecithin listed in ingredients statement but soy is not mentioned in the contains statement..
Details
Source
Food Recall
External ID
F-0788-2021
Action Date
2021-07-28
Status
Terminated
Category
food
Product Description
Heidi's Brownies is packaged in saran wrap in a plastic bag with a twist tie, 3 oz (85g). Label is read in parts: "***Heidi's ~~~ Brownies ~~~ *Malted barley wheat flour, cane sugar, water, chocolate chips (unsweetened chocolate, sugar, dextrose, soy lecithin (an emulsifier)(may contain milk), Non-GMO Canola oil, cocoa, apple cider vinegar, vanilla ***almond ext (May Contains Nuts), sodium bicarbonate, cinnamon, sea salt, demerara sugar ***Contains: Wheat, almonds *** Heidis Pie in the Sky Talent, OR 97540 ***".
Lot/Code Info: Best Used by Date or Freeze: 5/18/21-6/22/21
Quantity Affected: 72 units
Reason for Recall
Soy Lecithin listed in ingredients statement but soy is not mentioned in the contains statement.
Distribution
distributed in OR only.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-06-18
Company
Talent, OR
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 19 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Heidi Remington has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Heidi Remington) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Heidi Remington have FDA actions?
Heidi Remington has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0788-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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