FDA Adverse Event
Malfunction
Summary report: N
PLATINUM 10 CONCENTRATOR 9153642104
MDR report key: 4813313
·
Received June 2, 2015
Report
- Report Number
- 1031452-2015-13919
- Event Type
- Malfunction
- Date Received
- June 2, 2015
- Report Date
- May 5, 2015
- Manufacturer
- INVACARE FLORIDA OPERATIONS
- Product Code
- CAW
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Narratives
Additional Manufacturer Narrative · 1
NO END USER INFORMATION PROVIDED. THE PRODUCT WAS EVALUATED AND REPAIRED BY AN INDEPENDENT REPAIR CENTER. A FOLLOW-UP WILL BE SENT IF ADDITIONAL INFORMATION IS RECEIVED.
Description of Event or Problem · 1
PER THE INDEPENDENT REPAIR CENTER, THE CUSTOMER ALLEGED PROBLEM IS THE ALARM WILL NOT FUNCTION. THE KEY FAILURE IS THE POWER SWITCH HAS A SHORT CIRCUIT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 355456 | PLATINUM 10 CONCENTRATOR 9153642104 | GENERATOR, OXYGEN, PORTABLE | CAW | INVACARE FLORIDA OPERATIONS | IRC10LX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |