RecallHawk

SABRE Aim & Fire Pepper Gel Spray with Training Canisters

Security Equipment Corporation, of Fenton, Missouri

Summary

CPSC recall: SABRE Aim & Fire Pepper Gel Spray with Training Canisters. By Security Equipment Corporation, of Fenton, Missouri. Hazard: The Sabre Aim & Fire Pepper Gel Spray canisters do not contain the red nozzle on top of the valve stem that is needed to deploy the product and will not deploy pepper gel spray when it is triggered. Also, the canisters can fail to spray in the defense of the individual during an emergency.. Remedy: Consumers should immediately stop using the recalled SABRE Aim &

Details

Source

CPSC Consumer Product Recall

External ID

9782

Action Date

2023-12-07

Status

Recalled

Category

consumer_product

Product Description

This recall involves SABRE Aim & Fire Pepper Gel with Training Canisters with model number SDP-G-03. The canisters look

Context & Analysis

This is a unclassified recall.

This was one of 26 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Security Equipment Corporation, of Fenton, Missouri 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 (Security Equipment Corporation, of Fenton, Missouri) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Security Equipment Corporation, of Fenton, Missouri have FDA actions?

Security Equipment Corporation, of Fenton, Missouri 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 "9782" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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