Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Aesculap Miethke Shunt System Recalled by Aesculap, Inc. Due to Aesculap Inc. (AIC (USA)) initiated a recall of...

Date: November 11, 2014
Company: Aesculap, Inc.
Status: Terminated
Source: FDA (Device)

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 Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of the brain into the peritoneum.

Quantity: 4

Why Was This Recalled?

Aesculap Inc. (AIC (USA)) initiated a recall of Miethke Shunt System accessories due to missing patients' labels for the miniNAV (FV660T). There are no patient injuries resulting from this issue.

Where Was This Sold?

This product was distributed to 2 states: OK, WI

Affected (2 states)Not affected

About Aesculap, Inc.

Aesculap, Inc. has 22 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report