Teleflex Medical recalls Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.

Recall date

January 10, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0705-2018

FDA classification

Class II

Brand / firm

Teleflex Medical

Sold / distributed

US only

Why it was recalled

The pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may instead contain RUSCH GREEN LITE MAC 2.

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 Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.