FDA Adverse Event
Injury
Summary report: N
UNKNOWN 20FR. PULL PEG
MDR report key: 144708
·
Received January 14, 1998
Report
- Report Number
- 1223688-1998-00001
- Event Type
- Injury
- Date Received
- January 14, 1998
- Date of Event
- December 1, 1997
- Report Date
- December 4, 1997
- Manufacturer
- BIPD DIV., CR BARD
- Product Code
- KNT
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
RN STATES UNK MODEL PEG WAS IN PLACE APPROX 1 YEAR. PT PRESENTED AS AN OUT PT FOR REMOVAL OF PEG DUE TO ABILITY TO TAKE ORAL FEEDING. WHEN PHY. WENT TO TRACTION REMOVE PEG THE DOME SEPARATED. PHY SCOPED PT AND DOME WAS NOTED IN PT'S STOMACH. PHY USED UNK MODEL FORCEP TO REMOVE DOME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | UNKNOWN 20FR. PULL PEG Implant | FEEDING - TUBE | KNT | BIPD DIV., CR BARD | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 82 YR | Required Intervention |