MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,06,07 report with the FDA on 2011-06-14 for HUDSON NIPPLE AND NUT ADAPTER 42555 manufactured by Teleflex Medical.
[20794566]
The event is reported as: complaint alleges that the oxygen leaked through the device. Complaint states that during the alleged leak; the pt rec'd less oxygen. A new device was successfully used and there was no consequence for the pt.
Patient Sequence No: 1, Text Type: D, B5
[20911723]
The device sample was not rec'd by the mfr at the time of this report. A f/u report will be sent when completion of investigation.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 3004365956-2011-00242 |
MDR Report Key | 2175868 |
Report Source | 01,06,07 |
Date Received | 2011-06-14 |
Date of Report | 2011-05-31 |
Date Mfgr Received | 2011-05-31 |
Device Manufacturer Date | 2010-05-01 |
Date Added to Maude | 2012-03-23 |
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 | JASMINE BROWN |
Manufacturer Street | PO BOX 12600 |
Manufacturer City | DURHAM NC 27709 |
Manufacturer Country | US |
Manufacturer Postal | 27709 |
Manufacturer Phone | 9193614124 |
Manufacturer G1 | TELEFLEX |
Manufacturer Street | AVE. TRANSFORMACION 5954 PARQUE INDUSTRIAL FINSA |
Manufacturer City | NUEVO LAREDO 88275 |
Manufacturer Country | MX |
Manufacturer Postal Code | 88275 |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HUDSON NIPPLE AND NUT ADAPTER |
Generic Name | NIPPLE AND NUT ADAPTER |
Product Code | CAX |
Date Received | 2011-06-14 |
Model Number | NA |
Catalog Number | 42555 |
Lot Number | 02E1001891 |
ID Number | NA |
Operator | OTHER |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL |
Manufacturer Address | NUEVO LAREDO MX |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2011-06-14 |