Device recall
Z-2637-2025: JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside…
FDA device recall · Class II · North American Rescue LLC.
Key facts
| Recall number (Z-number) | Z-2637-2025 |
|---|---|
| Recall event | 97308 |
| 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… |
| Product code | DXC |
| Recalling firm | North American Rescue LLC. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K123194 |
| FEI number | 3005034064 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database