FDA Adverse Event
Other
Summary report: N
NA
MDR report key: 226447
·
Received June 3, 1999
Report
- Report Number
- 2953127-1999-00004
- Event Type
- Other
- Date Received
- June 3, 1999
- Date of Event
- April 7, 1999
- Report Date
- May 27, 1999
- Manufacturer
- NA
- Product Code
- GEI
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
NA
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | NA | NA | GEI | NA | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |