FDA recall record

Parker Trach-Vac Endotracheal Tubes recall — FDA Z-2243-2016

Parker Medical announces a voluntary field action for the Parker Trach-Vac Endotracheal Tubes - (Endotracheal tube,with Parker Flex-Tip,Sub-Glottic…

Class IIclassification
Z-2243-2016official record ID
Jul 27, 2016report date

Recall record at a glance

Official recordZ-2243-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmParker Medical
Report dateJul 27, 2016
Recall initiation dateJun 2, 2016
Quantity5,500 units
LocationHighlands Ranch, CO, United States

Official product description

Parker Trach-Vac Endotracheal Tubes. Tyvek pouches, 10 per box. Product Usage: The product is an endotracheal tube with sub-glottic suction channel to remove secretions. It is used for intubating patients and used with a ventilator to provide oxygen or anesthetic agents to the patient.

Why the product was recalled

Parker Medical announces a voluntary field action for the Parker Trach-Vac Endotracheal Tubes - (Endotracheal tube,with Parker Flex-Tip,Sub-Glottic Suction, High Volume low Pressure) due to tube kinking during use.

Distribution information

US Nationwide Distribution in the states of KY, MO, FL, TN, and TX.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

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