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Aesculap, Inc. recalls Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke Shunt System is inte
Recalled June 11, 2014 · FDA recall Z-1676-2014 · Aesculap
Hazard
AIC (USA) received information regarding 3 complaints in which the deflector did not move freely on the ventricular catheter. · FDA Class II
Units
48
Sold at
US Distribution including the states of PA, KY, NY, RI, SC, KS, TX, CT, TN and WA.
Description
AIC (USA) received information regarding 3 complaints in which the deflector did not move freely on the ventricular catheter.
Product
Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.
Manufacturer(s)
Aesculap, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →