Aesculap, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0502-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

The Dual Switch Valve is used for fluid drainage from the ventricles into the peritoneum, in cases of hydrocephalus.

Product Classification:

Class II

Date Initiated: October 24, 2014

Date Posted: December 10, 2014

Recall Number: Z-0502-2015

Event ID: 69600

Reason for Recall:

Aesculap Inc. (AIC (USA)) initiated a recall of Miethke Shunt System, Dual Switch Valve, due to incorrect product labeling on three units. The incorrect product labeling was the wrong expiration date, 2024-09, on the inner labeling of the sterile bag. However, the expiration date on the outer box was correct. No patient injuries were reported as a result of this issue.

Status: Terminated

Product Quantity: 1

Code Information:

Item Number FV129 Lot Number 4506244166 Serial Number A10150

Distribution Pattern:

US Distribution in Kansas only.

Voluntary or Mandated:

Voluntary: Firm initiated