Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units
Summary
CPSC recall: Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units. By Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.), of Houston, Texas. Hazard: The unit's serial plate can have incorrect electrical ratings which can lead to incorrect wirings being used, posing a fire hazard.. Remedy: Consumers should not attempt to open the outside electrical panel of the recalled air conditioning and heat pump units, and immediately contact
Details
Source
CPSC Consumer Product Recall
External ID
9968
Action Date
2024-06-13
Status
Recalled
Category
consumer_product
Product Description
This recall involves Amana, Daikin, and Goodman branded packaged air conditioners and heat pumps. The recalled units are
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.
Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.), of Houston, Texas has 2 FDA actions in our database, including 2 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 (Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.), of Houston, Texas) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.), of Houston, Texas have FDA actions?
Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.), of Houston, Texas 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 "9968" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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