MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-10-02 for PERITONEAL DIALYSIS CATHETER manufactured by .
[4914682]
Pt had a gtube and a peritoneal dialysis catheter. Was on tube feeds and had medication orders to be given via gtube. Rn inadvertently administered feeds/meds via peritoneal catheter instead of the gtube.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5038520 |
MDR Report Key | 4152623 |
Date Received | 2014-10-02 |
Date of Report | 2014-10-02 |
Date Added to Maude | 2014-10-10 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | UNKNOWN |
Health Professional | 0 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PERITONEAL DIALYSIS CATHETER |
Generic Name | PERITONEAL DIALYSIS CATHETER |
Product Code | FKO |
Date Received | 2014-10-02 |
Operator | HEALTH PROFESSIONAL |
Device Sequence No | 1 |
Device Event Key | 0 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Life Threatening; 3. Required No Informationntervention | 2014-10-02 |