Evaporator coil drain pans installed with residential condensing gas furnaces in an up-flow configuration
Goodman Manufacturing Company L.P., of Houston, Texas (evaporator coils)
Summary
CPSC recall: Evaporator coil drain pans installed with residential condensing gas furnaces in an up-flow configuration. By Goodman Manufacturing Company L.P., of Houston, Texas (evaporator coils). Hazard: The molded plastic drain pan located at the bottom of the evaporator coil, when installed with a residential condensing gas furnace in an up-flow configuration, can overheat, melt, and deform, posing a fire hazard.. Remedy: Contact Goodman Manufacturing Company to register for the free repair.
Details
Source
CPSC Consumer Product Recall
External ID
9177
Action Date
2021-11-18
Status
Recalled
Category
consumer_product
Product Description
This recall involves evaporator coil drain pans paired with residential condensing gas furnaces that are installed in a
Context & Analysis
This is a unclassified recall.
This was one of 7 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Goodman Manufacturing Company L.P., of Houston, Texas (evaporator coils) 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 (Goodman Manufacturing Company L.P., of Houston, Texas (evaporator coils)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Goodman Manufacturing Company L.P., of Houston, Texas (evaporator coils) have FDA actions?
Goodman Manufacturing Company L.P., of Houston, Texas (evaporator coils) 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 "9177" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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