FDA Adverse Event
Injury
Summary report: N
SEQUENTIAL COMPRESSION SLEEVE
MDR report key: 85407
·
Received July 2, 1996
Report
- Report Number
- 85407
- Event Type
- Injury
- Date Received
- July 2, 1996
- Date of Event
- April 24, 1996
- Report Date
- June 3, 1996
- Manufacturer
- KENDALL CO.
- Product Code
- JOW
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- CO, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
PT CAME FROM OR WITH THIGH HIGH ANTIEMBOLISM HOSE ON AND CO SCD THIGH HIGH OVER THAT. PT C/O OF RT ANKLE PAIN- FOUND HOSE BUNCHED UP AROUND ANKLE WITH LARGE INDENTED REDDENED AREA DORSAL ASPECT OF ANKLE, SCD'S WERE DC'D, ANTIEMBOLISM STOCKING REMOVED. LAST DOCUMENTATION IN CHART 4/25/96 AT 1945- PINK 3" TEARDROP SHAPE, ANT. SURFACE RT ANKLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SEQUENTIAL COMPRESSION SLEEVE | COMPRESSION STOCKING | JOW | KENDALL CO. | 5320 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 37 YR | Required Intervention |