FDA Adverse Event
Malfunction
Summary report: N
T:SLIM INSULIN DELIVERY SYSTEM
MDR report key: 10718192
·
Received October 22, 2020
Report
- Report Number
- 3013756811-2020-118296
- Event Type
- Malfunction
- Date Received
- October 22, 2020
- Date of Event
- October 2, 2020
- Report Date
- October 22, 2020
- Manufacturer
- TANDEM DIABETES CARE
- Product Code
- LZG
- UDI-DI
- 00852162004545
- PMA / PMN Number
- K111210
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
NO PRODUCT WAS RETURNED FOR EVALUATION. SHOULD NEW RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
Description of Event or Problem · 1
IT WAS REPORTED THAT INTERMITTENT OCCLUSION ALARMS OCCURRED. CUSTOMER CLEARED THE ALARM AND RESUMED INSULIN DELIVERY. SYSTEM CHECK WITH TANDEM TECHNICAL SUPPORT COULD NOT BE COMPLETED AT THE TIME OF CALL; HOWEVER, MULTIPLE ATTEMPTS WERE MADE BY TECHNICAL SUPPORT TO FOLLOW UP WITH THE CUSTOMER, BUT NO RESPONSE WAS RECEIVED. CUSTOMER'S BLOOD GLUCOSE WAS 150-398 MG/DL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1184289 | T:SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES CARE | 004628 | 00852162004545 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 15 YR |