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CARDINAL HEALTH

Cardinal Health 200, LLC · Model SEN23LPUC2 · UDI-DI 10195594046972

OGH Prescription
0
510(k) clearances
18
Adverse events
4
Recalls
15
Facilities

Description

LARYNGOSCOPY PACK

Recalls

DateFirmReason
2024-11-08Cardinal Health 200, LLCPotential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
2024-11-08Cardinal Health 200, LLCPotential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
2019-11-27Flexicare Medical Ltd.The firm has received reports that the spring/washer/bearing components in the block of the laryngoscope blade become loose and separated from the device. If the blade is disengag
2019-11-27Flexicare Medical Ltd.The firm has received reports that the spring/washer/bearing components in the block of the laryngoscope blade become loose and separated from the device. If the blade is disengag

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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.