Lantis system (pre-2003), Model #5835991 - Product Usage: Lantis Treatstation is to allow the radiation therapist to del
FDA device recall Z-2198-2019 · posted 2019-08-06 · Terminated
Recall details
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Reason for recall
- Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability
- Action taken
- We strongly recommend the following: Disable Remote Desktop Protocol (RDP) or close port 3389/tcp Ensure you have appropriate backups and system restoration procedures. If you have any questions or require assistance, please contact our service organization at 1-800-888-7436.
- Root cause
- Other
- Status
- Terminated
- Product code
- IYE
- 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
- Date initiated
- 2019-07-10
- Date posted
- 2019-08-06
- Date terminated
- 2020-06-03
- Location
- Malvern, PA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| ONCOR EXPRESSION (K060226) | Siemens Medical Solutions USA, Inc. | 2006-03-15 |