FDA Adverse Event
Malfunction
Summary report: N
FERNO SQUADMATE
MDR report key: 39679
·
Received September 6, 1996
Report
- Report Number
- 1523574-1996-00061
- Event Type
- Malfunction
- Date Received
- September 6, 1996
- Report Date
- September 6, 1996
- Manufacturer
- FERNO-WASHINGTON INC
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- NO INFORMATION
Narratives
Additional Manufacturer Narrative · 1
H-6 (86 OTHER) UNIT INSPECTED BY INDEPENDENT SERVICE AGENT - METHOD UNK.
Description of Event or Problem · 1
CUSTOMER CLAIMS TO HAVE HAD INCIDENTS OF CLOT FOLDING. NO INJURIES REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FERNO SQUADMATE | AMBULANCE COT | FPO | FERNO-WASHINGTON INC | 93-ES | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO |