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Curaplex

BOUND TREE MEDICAL, LLC · Model 021169-1S · UDI-DI 00815277028264

BTQ
10
510(k) clearances
313
Adverse events (3 deaths)
2
Recalls
127
Facilities

Description

Curaplex Nasopharyngeal Airway Kit incl 6 Airways - 20 Fr - 24 Fr - 28 Fr- 30 Fr - 32 Fr and 34 Fr

Recalls

DateFirmReason
2024-07-18Smiths Medical ASD Inc.Uncertainty in the seal integrity of the sterile packaging.
2017-01-13Teleflex MedicalLabeling error

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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.