MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-24 for FLEXITRUNK INFANT NASAL TUBING BC191 manufactured by Fisher & Paykel Healthcare Ltd.
[159518848]
(b)(4). The complaint bc191 flexitrunk nasal tubing is currently en route to fisher & paykel healthcare (b)(4) for further investigation. We will provide a follow up report upon the completion of our investigation.
Patient Sequence No: 1, Text Type: N, H10
[159518849]
A hospital in (b)(6) reported via a fisher & paykel healthcare (f&p) field representative that a flexitrunk infant nasal tube had a split in the tubing. No patient consequence was reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9611451-2015-00709 |
MDR Report Key | 8824419 |
Date Received | 2019-07-24 |
Date of Report | 2019-06-26 |
Date Mfgr Received | 2019-09-09 |
Device Manufacturer Date | 2019-01-29 |
Date Added to Maude | 2019-07-24 |
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 | MS FARANAK GOMAROONI |
Manufacturer Street | 173 TECHNOLOGY DRIVE SUITE 100 |
Manufacturer City | IRVINE CA 926182216 |
Manufacturer Country | US |
Manufacturer Postal | 926182216 |
Manufacturer Phone | 9494534000 |
Manufacturer G1 | FISHER & PAYKEL HEALTHCARE LTD |
Manufacturer Street | 15 MAURICE PAYKEL PLACE EAST TAMAKI |
Manufacturer City | AUCKLAND, 2013 |
Manufacturer Country | NZ |
Manufacturer Postal Code | 2013 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | FLEXITRUNK INFANT NASAL TUBING |
Generic Name | BZO |
Product Code | BZO |
Date Received | 2019-07-24 |
Model Number | BC191 |
Catalog Number | BC191 |
Lot Number | 2100688116 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | FISHER & PAYKEL HEALTHCARE LTD |
Manufacturer Address | 15 MAURICE PAYKEL PLACE EAST TAMAKI AUCKLAND, 2013 NZ 2013 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-07-24 |