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Aesculap, Inc. recalls Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt system is intended to shut cerebrosp
Recalled February 26, 2014 · FDA recall Z-0989-2014 · Aesculap
Hazard
The accuracy is out of specification for the Aesculap proSA Adjustment Disc Size L. · FDA Class II
Units
79
Sold at
Worldwide Distribution - US Distribution including the states of AZ, MD, MA, WI, MI, MN, DE, KS, and FL., and the countries of Australia, Germany, Great Britain, Norway and Japan.
Description
The accuracy is out of specification for the Aesculap proSA Adjustment Disc Size L.
Product
Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment 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 →