MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1998-11-10 for GASTROSTOMY CATHETERS E3314 manufactured by Rusch, Inc..
[144651]
Leakage occurred around the tube insertion. The dr took off the tape, pulled the tube, and found that the balloon had burst.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2429473-1998-00071 |
MDR Report Key | 197205 |
Report Source | 05 |
Date Received | 1998-11-10 |
Date of Report | 1998-11-10 |
Date of Event | 1998-07-23 |
Date Mfgr Received | 1998-10-28 |
Date Added to Maude | 1998-11-18 |
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 | GASTROSTOMY CATHETERS |
Generic Name | TRIPLE-PORT GASTROSTOMY CATHETERS |
Product Code | KDH |
Date Received | 1998-11-10 |
Model Number | NA |
Catalog Number | E3314 |
Lot Number | UNK |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 191596 |
Manufacturer | RUSCH, INC. |
Manufacturer Address | 2450 MEADOWBROOK PKWY. DULUTH GA 30096 US |
Baseline Brand Name | TRIPLE-PORT GASTROSTOMY CATHETERS |
Baseline Generic Name | GASTROSTOMY CATHETER |
Baseline Model No | NA |
Baseline Catalog No | E3314 |
Baseline ID | NA |
Baseline Device Family | GASTROSTOMY CATHETER |
Baseline Shelf Life [Months] | NA |
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. Required No Informationntervention | 1998-11-10 |