Armstrong Air and Air Ease single stage gas furnaces
Allied Air Enterprises LLC, of West Columbia, South Carolina
Summary
CPSC recall: Armstrong Air and Air Ease single stage gas furnaces. By Allied Air Enterprises LLC, of West Columbia, South Carolina. Hazard: A component inside the furnace was improperly assembled, causing the furnace to produce high levels of carbon monoxide (CO) under certain operating conditions, which poses a risk of CO poisoning to the consumer.. Remedy: Contact Allied Air Enterprises to schedule a free in-home repair by an authorized technician who will replace the incorrect component. Alli
Details
Source
CPSC Consumer Product Recall
External ID
9642
Action Date
2023-06-08
Status
Recalled
Category
consumer_product
Product Description
This recall involves 96% efficiency gas furnaces under the ARMSTRONG and AIREASE brand names with the model numbers A96U
Context & Analysis
This is a unclassified recall.
This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Allied Air Enterprises LLC, of West Columbia, South Carolina has 2 FDA actions in our database, including 1 recall.
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 (Allied Air Enterprises LLC, of West Columbia, South Carolina) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Allied Air Enterprises LLC, of West Columbia, South Carolina have FDA actions?
Allied Air Enterprises LLC, of West Columbia, South Carolina has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9642" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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