Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Recalled by Aesculap, Inc. Due to The accuracy is out of specification for the...
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 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.
Quantity: 79
Why Was This Recalled?
The accuracy is out of specification for the Aesculap proSA Adjustment Disc Size L.
Where Was This Sold?
This product was distributed to 9 states: AZ, DE, FL, KS, MD, MA, MI, MN, WI
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