Medical device recalls Moderate risk

Teleflex Medical recalls Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical.

Recall date
August 24, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0246-2016
FDA classification
Class II
Brand / firm
Teleflex Medical
Sold / distributed
Worldwide Distribution -- U.S. Nationwide; International Distribution: Argentina, Austria, Belgium, Belgrade, Cameroon, Canada, Chile, Costa Rica, Croatia, Czech Republic, Ecuador, Denmark, Estonia, Finland, France, French Polynesia, Great Britain, Greece, Guyana, Hong Kong, Ireland, Italy, Jordan,…

Why it was recalled

Due to reports of the plastic coating of the stylet splitting and/or breaking off of the stylet.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical.

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