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Teleflex Medical recalls Rusch EasyCath Kit
Recalled August 7, 2019 · FDA recall Z-2086-2019 · Teleflex Medical
Hazard
Potential for product not to be sterile. · FDA Class II
Units
3,700 devices
Sold at
Nationwide distribution to CA, FL, IL, NC, NJ, OH, OK, TX.
Description
Potential for product not to be sterile.
Product
Rusch EasyCath Kit
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →