FDA Adverse Event
Injury
Summary report: N
PROD TEST BRAND
MDR report key: 4987491
·
Received August 8, 2015
Report
- Report Number
- 2954323-2015-11111
- Event Type
- Injury
- Date Received
- August 8, 2015
- Date of Event
- August 8, 2015
- Report Date
- August 8, 2015
- Manufacturer
- ABBOTT DIABETES CARE INC.
- Product Code
- DFD
- PMA / PMN Number
- K12345678
- Report Source
- Manufacturer report
- Reporter Location
- MD, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
ADDING TEXT AT POINT OF REDACTION - THEN REDACTING.
Description of Event or Problem · 1
REDACTING IN PROD
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 521175 | PROD TEST BRAND | PROD DEVICE TYOE | DFD | ABBOTT DIABETES CARE INC. | M12345 | L12345 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 30 YR | Congenital Anomaly| L | CONCOMMITANT PROD MED PRODUCT - PROD REDAC |