MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2010-05-28 for N/A 11165 manufactured by Ascent Halthcare Solutions.
[1506763]
It was reported that the device would not hold pressure. No patient injury was reported.
Patient Sequence No: 1, Text Type: D, B5
[8628382]
At the time of this report the device investigation has not been completed. Once the investigation is completed a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1056128-2010-00026 |
MDR Report Key | 1702506 |
Report Source | 05,06,07 |
Date Received | 2010-05-28 |
Date of Report | 2010-07-15 |
Date Mfgr Received | 2010-06-18 |
Device Manufacturer Date | 2009-11-30 |
Date Added to Maude | 2011-04-08 |
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 | MS. MOIRA BARTON-VARTY |
Manufacturer Street | 10232 S. 51ST STREET |
Manufacturer City | PHOENIX AZ 85044 |
Manufacturer Country | US |
Manufacturer Postal | 85044 |
Manufacturer Phone | 4807635300 |
Manufacturer G1 | ASCENT HALTHCARE SOLUTIONS |
Manufacturer Street | 5307 GREAT OAK DRIVE |
Manufacturer City | LAKELAND FL 33815 |
Manufacturer Country | US |
Manufacturer Postal Code | 33815 |
Single Use | 3 |
Remedial Action | RC |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | N/A |
Generic Name | N/A |
Product Code | NMF |
Date Received | 2010-05-28 |
Returned To Mfg | 2010-05-17 |
Model Number | 11165 |
Catalog Number | 11165 |
Lot Number | 878402 |
Device Expiration Date | 2010-11-30 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ASCENT HALTHCARE SOLUTIONS |
Manufacturer Address | 5307 GREAT OAK DRIVE LAKELAND FL 33815 US 33815 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2010-05-28 |