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Curaplex

BOUND TREE MEDICAL, LLC · Model 8600-01198 · UDI-DI 00817617020587

OGL Prescription
0
510(k) clearances
13
Adverse events
1
Recalls
15
Facilities

Description

*Custom* Armstrong Ambulance HT70 Vent Circuit Kit

Recalls

DateFirmReason
2011-10-17Vital Signs Devices, a GE Healthcare CompanyPovidone Iodine Pads included in the Vital Signs Broselow Pediatric Emergency Kit may be contaminated with Elizabethkinga meningoseptica.

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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.