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HUDSON RCI

TELEFLEX INCORPORATED · Model IPN041676 · UDI-DI 04026704594511

BZB Prescription
8
510(k) clearances
25
Adverse events (1 deaths)
1
Recalls
36
Facilities

Description

Oxygen Catheter

Recalls

DateFirmReason
2024-11-273B Medical, Inc.The devices were inadvertently shipped after their expiration date.

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

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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.