FDA Adverse Event
Summary report: N
DAILY ACTIVITY ASSIST DEVICES
MDR report key: 4123430
·
Received September 26, 2014
Report
- Report Number
- 1531186-2014-04493
- Date Received
- September 26, 2014
- Report Date
- September 6, 2014
- Manufacturer
- SUN ZING PLASTIC IRONWARE
- Product Code
- IKX
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IS
- Reporter Occupation
- MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Narratives
Description of Event or Problem · 1
DEALER ALLEGES THAT HIS CUSTOMER RETURNED THE 218-3 GRAB BARS DUE TO SUCTION CUPS NOT HOLDING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 600068 | DAILY ACTIVITY ASSIST DEVICES | 890.5050 | IKX | SUN ZING PLASTIC IRONWARE | 218-3 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |