Home › NORTH AMERICAN RESCUE, LLC › NAR Kit
NAR Kit
NORTH AMERICAN RESCUE, LLC · Model 85-0740 · UDI-DI 00842209110599
OHO
Prescription
0
510(k) clearances
5
Adverse events
1
Recalls
235
Facilities
Description
KIT, TCCC SKILLS/IFAK COMBO; This kit contains item(s) labeled MRI unsafe.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-07 | INTEGRATED MEDCRAFT LLC | Devices could potentially contain an occluded or partially occluded Guedel Airway tip. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
