FDA Adverse Event
Death
Summary report: N
SONATA TUB
MDR report key: 288751
·
Received August 9, 2000
Report
- Report Number
- 9611530-2000-00023
- Event Type
- Death
- Date Received
- August 9, 2000
- Date of Event
- May 26, 2000
- Report Date
- July 7, 2000
- Manufacturer
- ARJO HOSPITAL EQUIPMENT AB
- Product Code
- ILJ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
THE FACILITY REPORTS THE PT WAS BROUGHT INTO THE SONATA TUB WITH THE MAXILIFT AND MESH SLING AND LOWERED INTO THE TUB. THE PT WAS LEFT UNATTENDED FOR AN UNSPECIFIED LENGTH OF TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SONATA TUB | BATHING SYSTEM | ILJ | ARJO HOSPITAL EQUIPMENT AB | 19XXXX | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 95 YR | Death |