MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2010-08-04 for DATEX-OHMEDA S/5 COMPACT AIRWAY MODULE E-CAIO manufactured by Ge Healthcare Finland, Oy.
[1631383]
A customer reported that a unit was failing a leak test. There is an indication in the complaint record that a death or serious injury may have occurred, however, no additional details are known at this time. Ge healthcare's investigation into the reported occurrence is still ongoing. A follow-up report will be issued when the investigation had been completed.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9610105-2010-00013 |
MDR Report Key | 1790246 |
Report Source | 06 |
Date Received | 2010-08-04 |
Date of Report | 2010-08-04 |
Date of Event | 2010-07-05 |
Date Mfgr Received | 2010-07-05 |
Date Added to Maude | 2010-08-13 |
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 | 0 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | DEBRA LAHR |
Manufacturer Street | 540 W NORTHWEST HWY |
Manufacturer City | BARRINGTON IL 600103076 |
Manufacturer Country | US |
Manufacturer Postal | 600103076 |
Manufacturer Phone | 8472774472 |
Manufacturer G1 | GE HEALTHCARE FINLAND, OY |
Manufacturer City | HELSINKI |
Manufacturer Country | FI |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DATEX-OHMEDA S/5 COMPACT AIRWAY MODULE E-CAIO |
Product Code | CCL |
Date Received | 2010-08-04 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | GE HEALTHCARE FINLAND, OY |
Manufacturer Address | HELSINKI FI |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Death | 2010-08-04 |