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Teleflex Medical recalls Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
Recalled March 7, 2018 · FDA recall Z-0705-2018 · Teleflex Medical
Hazard
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. · FDA Class II
Units
2140 units
Sold at
US only
Description
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.
Product
Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →