FDA Adverse Event
Other
Summary report: N
KENDRICK EXTRICATION DEVICE
MDR report key: 549527
·
Received March 30, 2004
Report
- Report Number
- 1523574-2004-00003
- Event Type
- Other
- Date Received
- March 30, 2004
- Report Date
- February 18, 2004
- Manufacturer
- FERNO-WASHINGTON, INC.
- Product Code
- IQK
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
CUSTOMER CLAIMS ONE WOODEN SLAT IS MISSING WHICH MAKES THE MEDICAL DEVICE UNSTABLE AND USELESS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KENDRICK EXTRICATION DEVICE | IMMOBILIZATION | IQK | FERNO-WASHINGTON, INC. | 125 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO |