FDA Adverse Event
Malfunction
Summary report: N
PIONEER MATTRESS 30"
MDR report key: 1760154
·
Received July 12, 2010
Report
- Report Number
- 1831750-2010-01501
- Event Type
- Malfunction
- Date Received
- July 12, 2010
- Date of Event
- June 21, 2010
- Report Date
- June 21, 2010
- Manufacturer
- STRYKER CORP, MEDICAL DIVISION
- Product Code
- IKY
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
IT HAS BEEN REPORTED THAT THE CUSTOMER PUT A PT ON THE PIONEER MATTRESS AND THE MATTRESS ABSORBED BLOOD.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PIONEER MATTRESS 30" | MATTRESS, FLOTATION THERAPY, NON-POWERED | IKY | STRYKER CORP, MEDICAL DIVISION | 0850030000 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |