Home › EMERGENCY MEDICAL PRODUCTS, INC. › Curaplex
Curaplex
EMERGENCY MEDICAL PRODUCTS, INC. · Model 8600-01404 · UDI-DI 00851772007328
0
510(k) clearances
5
Adverse events
1
Recalls
236
Facilities
Description
*Custom* Lycoming County Public IFAK Basic
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.