FDA Adverse Event
Other
Summary report: N
MX-PRO IT COT
MDR report key: 1952133
·
Received December 29, 2010
Report
- Report Number
- 1831750-2010-05310
- Event Type
- Other
- Date Received
- December 29, 2010
- Date of Event
- December 1, 2010
- Report Date
- December 1, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIV.
- Product Code
- INK
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NC, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE COTS IN A VEHICLE ACCIDENT NEED TO BE INSPECTED. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MX-PRO IT COT | STRETCHER, WHEELED | INK | STRYKER CORP., MEDICAL DIV. | 6081 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |