FDA recall record

Teleflex Medical HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product recall — FDA Z-0703-2020

The tracheal and brochial swivel connectors are incorrectly labeled.

Class IIclassification
Z-0703-2020official record ID
Dec 25, 2019report date

Recall record at a glance

Official recordZ-0703-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTeleflex Medical
Report dateDec 25, 2019
Recall initiation dateOct 30, 2019
Quantity53 units
LocationMorrisville, NC, United States

Official product description

HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial Tubes are intended for use in Thoracic surgery, brochospirometry, adminitration of endobronchial anesthesia and other uses commonly requiring endobronchial intubation. The Sheridan Endobronchial tube is indicated for main stem bronchus intubation and allows for selective inflation or deflation of either lung.

Why the product was recalled

The tracheal and brochial swivel connectors are incorrectly labeled.

Distribution information

US Nationwide distribution in the states of CT, OK, LA, IL, GA, NY, CA, MT, MI, MA, FL.

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: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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