Junctional Emergency Treatment Tool (North American Rescue) – Manufacturing Defect (2025)

Check Your Product

According to the U.S. Food and Drug Administration (FDA)

Reason for Recall

As stated by FDA

Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use.

Recommended Action

Per FDA guidance

On 7/1/2025, recall notices were emailed to customers who were asked to do the following: 1) Quarantine the junctional emergency treatment tools. 2) Discontinue use and distribution. 3) Complete and return the response form via email to recalls@narescue.com In addition, if you have further distributed affected products, identify your customers and notify them of this recall. Your notification to your customers may be enhanced by including a copy of the recall notice. Instruct your customers to return affected product to you and then you will coordinate return with the recalling firm. This recall should be carried out to the user level. If you have questions contact the firm's customer service at 1-888-689-6277