LANTIS Commander, LANTIS Commander 6.1, LANTIS 8.3 Commander, LANTIS System, LANTIS 6.1 Complete, LANTIS 6.1 Essential,
FDA device recall Z-2151-2011 · posted 2011-05-06 · Terminated
Recall details
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Reason for recall
- There is a potential safety issue in regard to data transfer between LANTIS OIS system and the hospital Information System (HIS) when the HL7 (ADT) interfact is used.
- Action taken
- Siemens sent an Urgent Medical Device Correction letter on March 23, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to include the Safety Advisory Notice in their LANTIS owner manual and contact there Siemens Service Engineer or Application Specialist or contact Lantis4.healthcare@siemens.com. For questions regarding this recall 925-602-8157.
- Root cause
- Other
- Status
- Terminated
- Product code
- LMB
- Quantity affected
- 47
- Distribution
- Nationwide Distribution.
- Date initiated
- 2011-03-23
- Date posted
- 2011-05-06
- Date terminated
- 2012-04-19
- Location
- Concord, CA
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