RecallHawk

AR-15 Chamber Lock Pro Firearm Locks

StopBox USA, of Spokane Valley, Washington

Summary

CPSC recall: AR-15 Chamber Lock Pro Firearm Locks. By StopBox USA, of Spokane Valley, Washington. Hazard: A manufacturing defect allows the recalled chamber locks to be forcibly removed, allowing unauthorized or unintended access to the firearm, posing a risk of serious injury or death.. Remedy: Consumers should immediately stop using the recalled AR-15 Chamber Lock Pro and secure their firearm using other means. Consumers should contact StopBox USA to receive a prepaid return shipping label and

Details

Source

CPSC Consumer Product Recall

External ID

10398

Action Date

2025-09-04

Status

Recalled

Category

consumer_product

Product Description

This recall involves certain AR-15 Chamber Lock Pro firearm locks shipped between June 2 and July 15, 2025. Consumers ca

Context & Analysis

This is a unclassified recall.

This was one of 10 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

StopBox USA, of Spokane Valley, Washington 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 (StopBox USA, of Spokane Valley, Washington) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does StopBox USA, of Spokane Valley, Washington have FDA actions?

StopBox USA, of Spokane Valley, Washington 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 "10398" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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