Evaporator coil drain pans
Summary
CPSC recall: Evaporator coil drain pans. By Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.) of Houston, Texas. Hazard: The molded plastic drain pan located at the bottom of the evaporator coil can overheat, melt and deform, posing a fire hazard.. Remedy: Consumers should contact Daikin Comfort Technologies Manufacturing L.P. (DCT) to determine whether your unit is included in this recall and to register for the free repair by a qualified technician. DCT
Details
Source
CPSC Consumer Product Recall
External ID
9821
Action Date
2024-01-11
Status
Recalled
Category
consumer_product
Product Description
This recall expansion includes certain units manufactured between January 2019 and February 2020 that were incorrectly m
Context & Analysis
This is a unclassified recall.
This was one of 9 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 "9821" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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