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Curaplex
BOUND TREE MEDICAL, LLC · Model 8600-01095 · UDI-DI 00815277029612
0
510(k) clearances
5
Adverse events
2
Recalls
236
Facilities
Description
*Custom* State of Kansas First Aid Trauma Kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-09-25 | INTEGRATED MEDCRAFT LLC | Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the sterile pad to degrade o |
| 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.