FDA Device Intelligence
HomeTELEFLEX INCORPORATED › HUDSON RCI

HUDSON RCI

TELEFLEX INCORPORATED · Model IPN044066 · UDI-DI 04026704597451

CAT Prescription
10
510(k) clearances
1,767
Adverse events (30 deaths)
6
Recalls
263
Facilities

Description

COMFORT FLO® Nasal Cannula

Recalls

DateFirmReason
2018-07-06Smiths Medical ASD Inc."Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.
2018-07-06Smiths Medical ASD Inc."Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.
2018-07-06Smiths Medical ASD Inc."Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.
2018-07-06Smiths Medical ASD Inc."Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.
2018-07-06Smiths Medical ASD Inc."Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.
2017-05-09Teleflex MedicalIncorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.