MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2000-10-30 for WHISTLE TIP URETERAL CATHETER 331104 manufactured by Rusch Mfg (uk) Ltd..
[168982]
It was reported that the catheter broke off inside the pt during ureteral stent placement. It was retrieved and another catheter was re-inserted without further incident.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8010095-2000-00094 |
MDR Report Key | 302815 |
Report Source | 05,06 |
Date Received | 2000-10-30 |
Date of Report | 2000-10-30 |
Date Mfgr Received | 2000-10-16 |
Date Added to Maude | 2000-11-03 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | KATRINA HALBIG, ADMINISTRATOR |
Manufacturer Street | 2450 MEADOWBROOK PKWY |
Manufacturer City | DULUTH GA 30136 |
Manufacturer Country | US |
Manufacturer Postal | 30136 |
Manufacturer Phone | 7706230816 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | WHISTLE TIP URETERAL CATHETER |
Generic Name | URETERAL CATHETER |
Product Code | FGF |
Date Received | 2000-10-30 |
Returned To Mfg | 2000-10-16 |
Model Number | NA |
Catalog Number | 331104 |
Lot Number | G990108 |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 293096 |
Manufacturer | RUSCH MFG (UK) LTD. |
Manufacturer Address | HALIFAX RD. CRESSEX INDUSTRIAL ESTATE HIGH WYCOMBE, BUCKINGHAMSHIRE UK |
Baseline Brand Name | WHITLE TIP URETERAL CATHETER |
Baseline Generic Name | URETERAL CATHETER |
Baseline Model No | NA |
Baseline Catalog No | 331104 |
Baseline ID | NA |
Baseline Device Family | URETHERAL CATHETER |
Baseline Shelf Life Contained | Y |
Baseline Shelf Life [Months] | 59 |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | Y |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2000-10-30 |