Lemon Almond Blueberry Bread, UPC 7 21762 76434 3, Net wt.3.5oz (98g). The sliced Lemon Blueberry Bread is wrapped in a
Summary
The FDA issued a Class III for Lemon Almond Blueberry Bread, UPC 7 21762 76434 3, Net wt.3.5oz (98g). The slice by Heidi Remington. Reason: Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products label does not declare Soy Lecithin.
Details
Source
Food Recall
External ID
F-0350-2023
Action Date
2023-02-22
Status
Terminated
Category
food
Product Description
Lemon Almond Blueberry Bread, UPC 7 21762 76434 3, Net wt.3.5oz (98g). The sliced Lemon Blueberry Bread is wrapped in a clear plastic shrink wrap. The label stated "***Lemon Almond Blueberry Bread* Malted barley wheat flour, milk, eggs, almonds...Contains: Wheat, eggs, milk, almonds***Heidi s Pie in the Sky, Talent, OR 97540***".
Lot/Code Info: Lot code 221227 and Best Used or Freeze By date of 1/6/23. Lot code 230104 and Best Used or Freeze By Date of 1/13/23. Lot code 230109 and Best Used or Freeze By Date of 1/17/23.
Quantity Affected: 76 packages
Reason for Recall
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products label does not declare Soy Lecithin
Distribution
distributed in Oregon.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-12
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 18 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-0350-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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