FDA Adverse Event
Injury
Summary report: N
SMITH'S CADD CASSETTES
MDR report key: 1820792
·
Received August 25, 2010
Report
- Report Number
- MW5017243
- Event Type
- Injury
- Date Received
- August 25, 2010
- Report Date
- August 25, 2010
- Manufacturer
- SMITH'S MEDICAL
- Product Code
- FPA
- Report Source
- Voluntary report
- Reporter Location
- PA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
PT COULD NOT REMOVE WHITE CAPS OFF OF END OF CASSETTE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SMITH'S CADD CASSETTES | 100ML CADD CASSETTES | FPA | SMITH'S MEDICAL | 187X10 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 56 YR | Congenital Anomaly| S |