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Curaplex
BOUND TREE MEDICAL, LLC · Model 670224-KIT · UDI-DI 00810071631900
0
510(k) clearances
5
Adverse events
1
Recalls
235
Facilities
Description
Curaplex Emergency Roadside Kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-07 | INTEGRATED MEDCRAFT LLC | Devices could potentially contain an occluded or partially occluded Guedel Airway tip. |
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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.