FDA Adverse Event
Malfunction
Summary report: N
MEDICAL ACTION LIGHT SHIELD, SEMI-RIGID, NON-STERILE
MDR report key: 6901947
·
Received September 28, 2017
Report
- Report Number
- 1836161-2017-00106
- Event Type
- Malfunction
- Date Received
- September 28, 2017
- Date of Event
- February 9, 2017
- Report Date
- September 28, 2017
- Manufacturer
- ASPEN SURGICAL PRODUCTS, CALEDONIA
- Product Code
- FTA
- PMA / PMN Number
- K020304
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
DEVICE NOT AVAILABLE.
Description of Event or Problem · 1
COMPLAINT (B)(4) ON ITEM NB8000. LIGHT SHIELD CRACKED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 680614 | MEDICAL ACTION LIGHT SHIELD, SEMI-RIGID, NON-STERILE | LIGHT SHIELD | FTA | ASPEN SURGICAL PRODUCTS, CALEDONIA | NB8000 | 114900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |