RecallHawk

System Sensor L-series low frequency Sounders and Strobes for residential apartments and commercial buildings

Honeywell International Inc., of Charlotte, North Carolina

Summary

CPSC recall: System Sensor L-series low frequency Sounders and Strobes for residential apartments and commercial buildings. By Honeywell International Inc., of Charlotte, North Carolina. Hazard: The sounders and strobes can malfunction and cause the fire alarm system to fail to alert consumers of a fire.. Remedy: Consumers should contact the firm to arrange for a free inspection and free repair..

Details

Source

CPSC Consumer Product Recall

External ID

9891

Action Date

2024-03-14

Status

Recalled

Category

consumer_product

Product Description

This recall involves all Honeywell System Sounder L-series Low Frequency Sounders, Sounder Strobes, and Compact Sounders

Context & Analysis

This is a unclassified recall.

This was one of 16 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Honeywell International Inc., of Charlotte, North Carolina 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 (Honeywell International Inc., of Charlotte, North Carolina) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Honeywell International Inc., of Charlotte, North Carolina have FDA actions?

Honeywell International Inc., of Charlotte, North Carolina 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 "9891" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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