RecallHawk

Leatherman Charge Plus and Charge Plus TTi Multi-Tools

Leatherman Tool Group Inc., of Portland, Oregon

Summary

CPSC recall: Leatherman Charge Plus and Charge Plus TTi Multi-Tools. By Leatherman Tool Group Inc., of Portland, Oregon. Hazard: The tip of the knife blade doesn't fully fold into the handle, posing a laceration hazard.. Remedy: Consumers should immediately stop using the recalled Charge Plus multi-tools and go to www.leatherman.com/pages/charge-recall to determine if their multi-tool falls within the scope of this recall. Consumers will not be asked for proof of purchase and will receive a pre-

Details

Source

CPSC Consumer Product Recall

External ID

10366

Action Date

2025-07-31

Status

Recalled

Category

consumer_product

Product Description

This recall involves Leatherman Charge Plus and Charge Plus TTi multi-tools. The Charge Plus multi-tools come in black a

Context & Analysis

This is a unclassified recall.

This was one of 21 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Leatherman Tool Group Inc., of Portland, Oregon 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 (Leatherman Tool Group Inc., of Portland, Oregon) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Leatherman Tool Group Inc., of Portland, Oregon have FDA actions?

Leatherman Tool Group Inc., of Portland, Oregon 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 "10366" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for consumer_product

Related Actions