MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2018-08-28 for HUDSON ISO-GARD HEPA LIGHT,CLEAN 28022 manufactured by Teleflex Medical.
[118547936]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
[118547937]
Customer complaint alleges "filter in use on expiratory side of vent (servo-i) using 880-36kit circuit. Filter works fine for a few hours and then restricts flow setting off vent alarm. (cont. ) clinician said it acts like a one way valve is closing inside filter. " it was reported there was no patient injury or consequence. Patient condition reported as "fine".
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8040412-2018-00225 |
MDR Report Key | 7822789 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2018-08-28 |
Date of Report | 2018-08-10 |
Date of Event | 2018-08-03 |
Date Mfgr Received | 2018-10-05 |
Date Added to Maude | 2018-08-28 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | KATHARINE TARPLEY |
Manufacturer Street | 3015 CARRINGTON MILL BLVD |
Manufacturer City | MORRISVILLE NC 27560 |
Manufacturer Country | US |
Manufacturer Postal | 27560 |
Manufacturer Phone | 9194334854 |
Manufacturer G1 | TELEFLEX MEDICAL |
Manufacturer Street | PO BOX 28, KAMUNTING INDUSTRIAL ESTATE |
Manufacturer City | PERAK, WEST MALAYSIA 34600 |
Manufacturer Country | MY |
Manufacturer Postal Code | 34600 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HUDSON ISO-GARD HEPA LIGHT,CLEAN |
Generic Name | FILTER, BACTERIAL, BREATHING-C |
Product Code | CAH |
Date Received | 2018-08-28 |
Catalog Number | 28022 |
Lot Number | UNKNOWN |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL |
Manufacturer Address | PERAK, WEST MALAYSIA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-08-28 |