RecallHawk

Crown Aruba IV (AWR Series) gas-fired hot water boilers

Crown Boiler Company LLC, of Philadelphia, Pennsylvania

Summary

CPSC recall: Crown Aruba IV (AWR Series) gas-fired hot water boilers. By Crown Boiler Company LLC, of Philadelphia, Pennsylvania. Hazard: The blocked vent switch (BVS) can fail to shut down the burners if the boilers are installed at altitudes above 2,000 feet and the vent system becomes blocked. In such an event, the boiler can emit excessive amounts of carbon monoxide into the building, posing a carbon monoxide (CO) poisoning hazard to consumers.. Remedy: Consumers with the recalled boilers sh

Details

Source

CPSC Consumer Product Recall

External ID

9897

Action Date

2024-03-21

Status

Recalled

Category

consumer_product

Product Description

This recall involves Crown Boiler Aruba IV (AWR Series) gas-fired hot water boilers powered by natural gas and LP (propa

Context & Analysis

This is a unclassified recall.

This was one of 11 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Crown Boiler Company LLC, of Philadelphia, Pennsylvania 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 (Crown Boiler Company LLC, of Philadelphia, Pennsylvania) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Crown Boiler Company LLC, of Philadelphia, Pennsylvania have FDA actions?

Crown Boiler Company LLC, of Philadelphia, Pennsylvania 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 "9897" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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