FDA Adverse Event Malfunction Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 3905213 · Received May 29, 2014

Report

Report Number
3007981285-2014-00862
Event Type
Malfunction
Date Received
May 29, 2014
Date of Event
May 3, 2014
Report Date
May 3, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

DURING FURTHER TROUBLESHOOTING REPORTER INFORMED TANDEM HE HAS BEEN REDUCING SOME OF HIS BASAL RATES WITHOUT DOCTORS APPROVAL.

Description of Event or Problem · 1

RECEIVED INFORMATION STATING PATIENT HAS BEEN EXPERIENCING HIGH BG'S (300+ MG/DL).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
317434 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628

Patients

Seq Age Sex Outcome Treatment
1 66 YR