FDA Device Intelligence
HomeNORTH AMERICAN RESCUE, LLC › NAR

NAR

NORTH AMERICAN RESCUE, LLC · Model 85-4520 · UDI-DI 00842209130467

OHO
0
510(k) clearances
5
Adverse events
1
Recalls
235
Facilities

Recalls

DateFirmReason
2026-07-07INTEGRATED MEDCRAFT LLCDevices 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 docs
Data 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.