PlainRecalls
FDA Devices Moderate Class II Terminated

MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.

Reported: November 18, 2015 Initiated: September 24, 2015 #Z-0265-2016

Product Description

MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.

Reason for Recall

Display freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user.

Details

Units Affected
15
Distribution
Distributed in PR and the states of MO, NC, GA, MS, LA, and KY.
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 15.
Why was this product recalled?
Display freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 18, 2015. Severity: Moderate. Recall number: Z-0265-2016.