FDA Adverse Event
Other
Summary report: N
POWER PRO AMBULANCE COT
MDR report key: 1032464
·
Received April 16, 2008
Report
- Report Number
- 1831750-2008-00071
- Event Type
- Other
- Date Received
- April 16, 2008
- Date of Event
- October 20, 2006
- Report Date
- March 18, 2008
- Manufacturer
- STRYKER CORP - MEDICAL DIV
- Product Code
- FPO
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- LA, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
CUSTOMER UNWILLING TO ALLOW STRYKER REP ACCESS TO COT.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE COT DID NOT CATCH ON THE SAFETY HOOK DUE TO ADMITTED USER-ERROR. IT WAS REPORTED THAT INJURY OCCURRED. THE CUSTOMER IS UNWILLING TO PROVIDE ANY FURTHER INFO REGARDING THE COT, THE USE, OR THE ALLEGED INJURY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | POWER PRO AMBULANCE COT | AMBULANCE COT | FPO | STRYKER CORP - MEDICAL DIV | 6500000000 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |