Modularis Variostar recall
MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.
Why was Modularis Variostar 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
model# 1157200
- Product
- MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 15
- Distribution
- Distributed in PR and the states of MO, NC, GA, MS, LA, and KY.
- Recall date
- November 18, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)