MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-24 for VERSAJET II CONSOLE 66800039 manufactured by Smith & Nephew Medical Ltd..
[185736613]
It was reported that during surgery the versajet ii did not suction. More than 30 minutes delay was reported and no backup device was available. The surgeon proceeded to complete the surgery without the device.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8043484-2020-00200 |
MDR Report Key | 9875296 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-24 |
Date of Report | 2020-03-24 |
Date of Event | 2020-03-06 |
Date Mfgr Received | 2020-03-06 |
Date Added to Maude | 2020-03-24 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | DR SARAH FREESTONE |
Manufacturer Street | 101 HESSLE ROAD |
Manufacturer City | HULL HU3 2BN |
Manufacturer Country | UK |
Manufacturer Postal | HU3 2BN |
Manufacturer Phone | 0447940038 |
Manufacturer G1 | SMITH & NEPHEW MEDICAL LTD. |
Manufacturer Street | 101 HESSLE ROAD |
Manufacturer City | HULL HU3 2BN |
Manufacturer Country | UK |
Manufacturer Postal Code | HU3 2BN |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VERSAJET II CONSOLE |
Generic Name | LAVAGE, JET |
Product Code | FQH |
Date Received | 2020-03-24 |
Catalog Number | 66800039 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITH & NEPHEW MEDICAL LTD. |
Manufacturer Address | 101 HESSLE ROAD HULL HU3 2BN UK HU3 2BN |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-24 |