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