RecallHawk

Apollo America 51000-600 Combination Smoke and Carbon Monoxide Detectors

Apollo America Inc., of Auburn Hills, Michigan

Summary

CPSC recall: Apollo America 51000-600 Combination Smoke and Carbon Monoxide Detectors. By Apollo America Inc., of Auburn Hills, Michigan. Hazard: The recalled detectors can malfunction and fail to alert consumers of a fire or carbon monoxide (CO) leak, posing a risk of smoke inhalation, carbon monoxide poisoning or death.. Remedy: Vivint is sending a free replacement detector to all known purchasers. Consumers should continue using the recalled detectors until they install the replacement detect

Details

Source

CPSC Consumer Product Recall

External ID

10302

Action Date

2025-06-05

Status

Recalled

Category

consumer_product

Product Description

This recall involves Apollo America Combination Smoke and Carbon Monoxide Detectors with model number 51000-600. The rec

Context & Analysis

This is a unclassified recall.

This was one of 24 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Apollo America Inc., of Auburn Hills, Michigan 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 (Apollo America Inc., of Auburn Hills, Michigan) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Apollo America Inc., of Auburn Hills, Michigan have FDA actions?

Apollo America Inc., of Auburn Hills, Michigan 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 "10302" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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