Frigidaire rear-controlled ranges
Summary
CPSC recall: Frigidaire rear-controlled ranges. By Electrolux Home Products, Inc. of Charlotte, North Carolina. Hazard: The control panel (user interface) on the ranges can detach from the unit, posing electrical shock and electrocution hazards.. Remedy: Consumers should immediately stop using the recalled Frigidaire rear-controlled ranges and contact Electrolux Group for a free repair/professional installation of a new control panel. Consumers should not use the range while awaiting the service
Details
Source
CPSC Consumer Product Recall
External ID
9852
Action Date
2024-02-15
Status
Recalled
Category
consumer_product
Product Description
This recall involves select Frigidaire brand rear-controlled ranges produced from October 2023 through November 2023 wit
Context & Analysis
This is a unclassified recall.
This was one of 12 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Electrolux Home Products, Inc. of Charlotte, North Carolina has 8 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a FDA 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 (Electrolux Home Products, Inc. of Charlotte, North Carolina) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Electrolux Home Products, Inc. of Charlotte, North Carolina have FDA actions?
Electrolux Home Products, Inc. of Charlotte, North Carolina has 8 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9852" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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