MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2014-10-23 for INTELLISPACE CRITICAL CARE & ANESTHESIA REV G.0 866148 manufactured by Philips Medical Systems.
[17947965]
When the start time of a one-time order is changed to an earlier time, then a later time, icca shows 2 pending interventions. There should be only 1 intervention listed. Users could mistakenly administer an extra intervention for a 1 time order. No patient harm occurred.
Patient Sequence No: 1, Text Type: D, B5
[18131229]
(b)(4). A follow up report will be submitted once the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1218950-2014-06175 |
MDR Report Key | 4392196 |
Report Source | 01,05,06 |
Date Received | 2014-10-23 |
Date of Report | 2014-10-08 |
Date Mfgr Received | 2014-10-08 |
Date Added to Maude | 2015-01-16 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | BETTY HARRIS |
Manufacturer Street | 3000 MINUTEMAN RD. |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal | 01810 |
Manufacturer Phone | 9786593311 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | INTELLISPACE CRITICAL CARE & ANESTHESIA REV G.0 |
Generic Name | NONE |
Product Code | NSX |
Date Received | 2014-10-23 |
Model Number | 866148 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS MEDICAL SYSTEMS |
Manufacturer Address | 3000 MINUTEMAN RD. ANDOVER MA 01810 US 01810 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2014-10-23 |