FDA Adverse Event
Injury
Summary report: N
ALLEGIANCE HEALTHCARE CORP.
MDR report key: 252140
·
Received December 1, 1999
Report
- Report Number
- 252140
- Event Type
- Injury
- Date Received
- December 1, 1999
- Date of Event
- October 31, 1999
- Report Date
- November 9, 1999
- Manufacturer
- ALLEGIANCE HEALTHCARE CORP.
- Product Code
- GBX
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Occupation
- INVALID DATA
Narratives
Description of Event or Problem · 1
DURING REMOVAL OF DRAIN TUBING, DRAIN TUBING BROKE LEAVING PART OF TUBING INSIDE PT. SURGERY WAS REQUIRED TO REMOVE BROKEN PIECE OF DRAIN TUBING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ALLEGIANCE HEALTHCARE CORP. Implant | JACKSON-PRATT DRAIN | GBX | ALLEGIANCE HEALTHCARE CORP. | HEMADUCT GOLD | 1990944 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 26 MO | Required Intervention |