LIMERICK, Pa.--(BUSINESS WIRE)--Feb. 12, 2014--
Teleflex Medical Incorporated has announced a worldwide voluntary recall
of its ISIS™ HVT™ Tracheal Tube Cuffed with Subglottic Secretion Suction
Port (with and without Preloaded Stylet). This recall is being conducted
because of complaints that the tracheal tube can kink during patient
use. If a tracheal tube kinks, it can deprive the patient of adequate
ventilation causing serious injury, including hypoxic injury and/or
anoxia.
The U.S. Food and Drug Administration (“FDA”) has classified this action
as a Class I recall. FDA defines class I recalls as “a situation in
which there is a reasonable probability that the use of or exposure to a
violative product will cause serious adverse health consequences or
death.”
Teleflex initiated this recall by a letter to its U.S. customers on
January 6, 2014. In accordance with the instructions provided in the
recall letter, customers should immediately discontinue use of the
recalled devices and return all unused ISIS products to Teleflex
Medical. The affected product codes are:
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Product Description
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Product Code
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction
Port, 6.0
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5-13012
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction
Port, 6.5
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5-13013
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction
Port, 7.0
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5-13014
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction
Port, 7.5
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5-13015
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction
Port, 8.0
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5-13016
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction
Port, 8.5
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5-13017
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction
Port, 9.0
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5-13018
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port
and Preloaded Stylet, 6.0
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5-14012
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port
and Preloaded Stylet, 6.5
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5-14013
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port
and Preloaded Stylet, 7.0
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5-14014
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port
and Preloaded Stylet, 7.5
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5-14015
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port
and Preloaded Stylet, 8.0
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5-14016
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port
and Preloaded Stylet, 8.5
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5-14017
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ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port
and Preloaded Stylet, 9.0
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5-14018
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A list of product and lot numbers affected by this recall, as well as
the original recall notice, can be found at Teleflex’s website:
Recall
Notice
Consumers with questions may contact the company at 1-866-804-9881; 8am
to 8pm, ET, Monday through Friday.
Any adverse reactions experienced with the use of these products, and/or
quality problems may also be reported to the FDA’s MedWatch Program by
phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at MedWatch,
FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch
website at www.fda.gov/medwatch.
About Teleflex Medical Incorporated
Teleflex Medical Incorporated is a subsidiary of Teleflex Incorporated
(NYSE:TFX). Teleflex Incorporated is a leading global provider of
specialty medical devices for a range of procedures in critical care and
surgery. Our mission is to provide solutions that enable healthcare
providers to improve outcomes and enhance patient and provider safety.
Headquartered in Limerick, PA, Teleflex employs approximately 11,400
people worldwide and serves healthcare providers in more than 140
countries. For additional information about Teleflex please refer to www.teleflex.com.

Source: Teleflex Medical Incorporated
Teleflex Medical Incorporated
Jake Elguicze
Treasurer and Vice
President, Investor Relations
610-948-2836