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Curaplex

BOUND TREE MEDICAL, LLC · Model 2-0211-8128 · UDI-DI 00810071636356

BTQ Prescription
10
510(k) clearances
312
Adverse events (3 deaths)
2
Recalls
126
Facilities

Description

Curaplex Select Nasopharyngeal Airway, 28 Fr, 7.0mm, Robertazzi Style, Latex Free, Sterile 10ea/bx

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.