FDA Adverse Event Injury Summary report: N

TANDEM T: SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3931588 · Received June 24, 2014

Report

Report Number
3007981285-2014-01461
Event Type
Injury
Date Received
June 24, 2014
Date of Event
May 24, 2014
Report Date
May 24, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE IS AVAILABLE FOR EVAL; HOWEVER, THE DEVICE HAS NOT BEEN RECEIVED. A F/U REPORT WILL BE FILED IF THE DEVICE IS RECEIVED.

Description of Event or Problem · 1

RECEIVED INFO STATING CUSTOMER RECEIVED MULTIPLE OCCLUSION ALARMS. REPORTEDLY, THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
367175 TANDEM T: SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628 M000534

Patients

Seq Age Sex Outcome Treatment
1 34 YR Other