Severity
Moderate
StopBox USA, of Spokane Valley, Washington issued this CPSC recall on September 4, 2025. Classified as Moderate severity. Approximately About 300 units are affected. The recall was issued because: A manufacturing defect allows the recalled chamber locks to be forcibly removed, allowing unauthorized or unintended ac…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
This CPSC action (record #25458) was formally reported on September 4, 2025. It is classified under Moderate severity, with a current status of Active. StopBox USA, of Spokane Valley, Washington is listed as the recalling firm. Federal records indicate About 300 units are affected.
The documented reason for this recall is: 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. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: 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… — consumers holding this product should act on that instruction rather than relying on general guidance.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 1 year old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Severity
Moderate
Units Affected
About 300
Related Recalls
6
0 from same agency
This recall involves certain AR-15 Chamber Lock Pro firearm locks shipped between June 2 and July 15, 2025. Consumers can find their shipping date by contacting StopBox by phone, email, or online at https://stopboxusa.com/pages/stopbox-ar-15-chamber-lock-recall. This is a device designed to lock into the chamber of an AR-15 style rifle and prevent it from firing. The product is made of anodized aluminum machined parts, was sold in red and black, and has five buttons that correspond to each finger. It has the StopBox "S" logo and "CHAMBER LOCK PRO AR-15" laser etched on the back of the product.
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.
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 instructions to return their recalled AR-15 Chamber Lock Pro for their choice of a full refund or replacement AR-15 Chamber Lock Pro.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 25458 |
| Date reported | September 4, 2025 |
| Date initiated | September 4, 2025 |
| Recalling firm | StopBox USA, of Spokane Valley, Washington |
| Units affected | About 300 |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
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Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
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Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).