MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1999-05-19 for GILSDORF GASTROSTOMY CATHETER E3430 manufactured by Rusch, Inc..
[129059]
It is alleged that the balloon inflation port plug popped out. The device had been in place for approx 1 month.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2429473-1999-00044 |
MDR Report Key | 224391 |
Report Source | 05 |
Date Received | 1999-05-19 |
Date of Report | 1999-05-18 |
Date of Event | 1999-05-17 |
Date Mfgr Received | 1999-05-17 |
Date Added to Maude | 1999-05-25 |
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 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | GILSDORF GASTROSTOMY CATHETER |
Generic Name | GASTROSTOMY CATHETER |
Product Code | KDH |
Date Received | 1999-05-19 |
Model Number | NA |
Catalog Number | E3430 |
Lot Number | 726030 |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 217594 |
Manufacturer | RUSCH, INC. |
Manufacturer Address | 2450 MEADOWBROOK PKWY. DULUTH GA 30096 US |
Baseline Brand Name | GILSDORF GASTROSTOMY CATHETER |
Baseline Generic Name | GASTROSTOMY CATHETER |
Baseline Model No | NA |
Baseline Catalog No | E3430 |
Baseline ID | NA |
Baseline Device Family | GASTROSTOMY CATHETER |
Baseline Shelf Life Contained | * |
Baseline Shelf Life [Months] | 59 |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K891371 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 1999-05-19 |