# FDA recall Z-2637-2025

> **North American Rescue LLC.** · Class II · device recall initiated 2025-07-01.

## Product

JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits:     KIT, TCCC Training- Complete (Modules 1-3), REF: 85-0550;  KIT, TCCC MODULE ONE - SKILLS, REF: 85-0519;  KIT, MULTI MISSION EXPEDITIONARY RESPONSE - MMERK, REF: 85-2420;  KIT, TCCC SKILLS/IFAK COMBO, REF: 85-0740,   KIT, TCCC/TECC MODULE ONE SKILLS REFILL, REF: 85-1900

## Reason for recall

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.

## Distribution

Worldwide - US Nationwide distribution in the states of SC, OK, ID, KY, VA, NV, IL, TX, CA, FL, LA, NY, LA, ME, PA, AR, AZ, AL, DE, MA, MS, HI, WA, MI, GA, NJ, UT, MD, OR, NC, NC, AL and the countries of KOR, JPN, BWA, SAU, BEL.

## Key facts

- **Recall number:** Z-2637-2025
- **Recalling firm:** North American Rescue LLC.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-01
- **Report date:** 2025-10-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Greer, SC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2637-2025

## Citation

> AI Analytics. FDA recall Z-2637-2025. Retrieved 2026-09-08 from https://api.ai-analytics.org/recall/Z-2637-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*