FDA Adverse Event
Death
Summary report: N
HOYER LIFTER
MDR report key: 285739
·
Received July 14, 2000
Report
- Report Number
- 2182598-2000-00028
- Event Type
- Death
- Date Received
- July 14, 2000
- Date of Event
- July 4, 1998
- Report Date
- July 14, 2000
- Manufacturer
- SUNRISE MEDICAL INC. / PCP HOYER DIVISION
- Product Code
- FSA
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- ND, US
- Reporter Occupation
- ATTORNEY
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THROUGH AN ATTORNEY LETTER THAT A HOYER LIFTER WAS INVOLVED IN AN INCIDENT. ATTORNEY UNWILLING TO GIVE SPECIFIC DETAILS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HOYER LIFTER | PATIENT LIFTER | FSA | SUNRISE MEDICAL INC. / PCP HOYER DIVISION | UNK | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Death |