Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Recalled by Aesculap, Inc. Due to AIC (USA) received information regarding 3 complaints in...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aesculap, Inc. directly.
Affected Products
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.
Quantity: 48
Why Was This Recalled?
AIC (USA) received information regarding 3 complaints in which the deflector did not move freely on the ventricular catheter.
Where Was This Sold?
This product was distributed to 10 states: CT, KS, KY, NY, PA, RI, SC, TN, TX, WA
About Aesculap, Inc.
Aesculap, Inc. has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report