MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2019-10-22 for FLEXITRUNK INFANT NASAL TUBING BC192 manufactured by Fisher & Paykel Healthcare Limited.
[177825828]
(b)(4). The complaint bc192 flexitrunk infant nasal tubing is en route to fisher & paykel healthcare (f&p) for evaluation. We will provide a follow up report upon completion of our investigation.
Patient Sequence No: 1, Text Type: N, H10
[177825829]
A healthcare facility in (b)(6) reported that a bc192 flexitrunk infant nasal tubing was damaged during patient use. There was no patient consequences.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9611451-2019-01005 |
MDR Report Key | 9222093 |
Report Source | FOREIGN,USER FACILITY |
Date Received | 2019-10-22 |
Date of Report | 2019-09-25 |
Date Mfgr Received | 2019-12-01 |
Device Manufacturer Date | 2018-04-26 |
Date Added to Maude | 2019-10-22 |
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 | 3 |
Event Location | 3 |
Manufacturer Contact | MS. FARANAK GOMAROONI |
Manufacturer Street | 173 TECHNOLOGY DR., SUITE 100 IRVINE |
Manufacturer City | CA 92618 |
Manufacturer Country | US |
Manufacturer Postal | 92618 |
Manufacturer Phone | 9494534000 |
Manufacturer G1 | FISHER & PAYKEL HEALTHCARE LIMITED |
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 | 3 |
Brand Name | FLEXITRUNK INFANT NASAL TUBING |
Generic Name | BZO |
Product Code | BZO |
Date Received | 2019-10-22 |
Returned To Mfg | 2019-11-28 |
Model Number | BC192 |
Catalog Number | BC192 |
Lot Number | 2100469322 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | FISHER & PAYKEL HEALTHCARE LIMITED |
Manufacturer Address | 15 MAURICE PAYKEL PLACE EAST TAMAKI AUCKLAND, 2013 NZ 2013 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-22 |