Lantis Commander recall
Lantis Commander, Model # 4503178 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the patient using…
Why was Lantis Commander recalled?
Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability
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?
Serial # 93-0759 93-0648 93-0662 93-1045 93-0574 93-0313 93-0501 93-0951 93-0667 93-0141 93-0786 93-0385 93-0799 93-0659 93-0861 ***added 8/14/19*** 93-0159 93-0878 93-0272 93-0596
- Product
- Lantis Commander, Model # 4503178 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the patient using…
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 15
- Distribution
- State WV NY PA FL OK FL NJ NY IL WY NY GA NY PA PA AL NJ NY ***updated 8/14/19*** OH NC
- Recall date
- August 14, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)