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RUSCH

TELEFLEX INCORPORATED · Model IPN041737 · UDI-DI 24026704009361

BTS Prescription

510(k) clearances

2,489

Adverse events (5 deaths)

Recalls

Facilities

Description

Double lumen bronchial tube White

Recalls

Date	Firm	Reason
2014-11-21	Teleflex, Inc.	Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21	Teleflex, Inc.	Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21	Teleflex, Inc.	Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21	Teleflex, Inc.	Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21	Teleflex, Inc.	Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21	Teleflex, Inc.	Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21	Teleflex, Inc.	Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21	Teleflex, Inc.	Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-11-21	Teleflex, Inc.	Customer complaints reporting that the cobb connector detached from the main connector prior to use.
2014-02-28	Teleflex Medical	The product may fail to achieve seal of right lung due to the cuff inflating to one side

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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.