RecallHawk

Residential atmospheric gas-fired boilers

Laars Heating Systems Company, of Rochester, New Hampshire

Summary

CPSC recall: Residential atmospheric gas-fired boilers. By Laars Heating Systems Company, of Rochester, New Hampshire. Hazard: The blocked vent temperature switch (BVTS) can malfunction, which can cause the release of gases, including carbon monoxide (CO), into consumers' homes, posing a risk of carbon monoxide poisoning.. Remedy: Consumers should immediately contact Laars Heating Systems Company to arrange to have a certified technician install repairs at no cost to the consumer. Consumers who

Details

Source

CPSC Consumer Product Recall

External ID

9342

Action Date

2022-06-30

Status

Recalled

Category

consumer_product

Product Description

This recall involves residential atmospheric gas-fired boilers manufactured from January 28, 2021 through January 12, 20

Context & Analysis

This is a unclassified recall.

This was one of 12 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Laars Heating Systems Company, of Rochester, New Hampshire 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 (Laars Heating Systems Company, of Rochester, New Hampshire) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Laars Heating Systems Company, of Rochester, New Hampshire have FDA actions?

Laars Heating Systems Company, of Rochester, New Hampshire 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 "9342" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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