FDA recall record

Siemens Medical Solutions USA MODULARIS VARIOSTAR recall — FDA Z-0265-2016

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

Class IIclassification
Z-0265-2016official record ID
Nov 18, 2015report date

Recall record at a glance

Official recordZ-0265-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSiemens Medical Solutions USA, Inc.
Report dateNov 18, 2015
Recall initiation dateSep 24, 2015
Quantity15
LocationMalvern, PA, United States

Official product description

MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.

Why the product was 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.

Distribution information

Distributed in PR and the states of MO, NC, GA, MS, LA, and KY.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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