Potter Electric Addressable Pull Stations Single/Dual Action
Summary
CPSC recall: Potter Electric Addressable Pull Stations Single/Dual Action. By Potter Electric Signal Company, LLC, of St. Louis, Mo.. Hazard: The pull handle on some units can fail to activate the fire alarm system when manually pulled, posing a risk of failure to alert consumers to a fire.. Remedy: Consumers should immediately contact Potter Electric or their fire alarm system dealers/installers for a free replacement. All known Potter Electric distributors and dealers/installers have been noti
Details
Source
CPSC Consumer Product Recall
External ID
9003
Action Date
2021-02-24
Status
Recalled
Category
consumer_product
Product Description
This recall involves Potter Electric Addressable Pull Stations. When manually pulled, these red-colored devices are inte
Context & Analysis
This is a unclassified recall.
This was one of 9 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Potter Electric Signal Company, LLC, of St. Louis, Mo. 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 (Potter Electric Signal Company, LLC, of St. Louis, Mo.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Potter Electric Signal Company, LLC, of St. Louis, Mo. have FDA actions?
Potter Electric Signal Company, LLC, of St. Louis, Mo. 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 "9003" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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