FDA Adverse Event
Malfunction
Summary report: N
TANDEM T: SLIM INSULIN DELIVERY SYS
MDR report key: 3952542
·
Received May 15, 2014
Report
- Report Number
- 3007981285-2014-00633
- Event Type
- Malfunction
- Date Received
- May 15, 2014
- Date of Event
- April 15, 2014
- Report Date
- April 15, 2014
- Manufacturer
- TANDEM DIABETES
- Product Code
- LZG
- PMA / PMN Number
- K111210
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
NO PRODUCT RETURNING FOR EVALUATION. ATTEMPTS WERE MADE TO OBTAIN ALL AVAILABLE INFO. SHOULD NEW INFO BECOME AVAILABLE, A FOLLOW UP MDR WILL BE SUBMITTED.
Description of Event or Problem · 1
RECEIVED INFO STATING CUSTOMER RECEIVED AN OCCLUSION ALARM. THERE WAS NO REPORTED IMPACT TO THE CUSTOMER'S BLOOD GLUCOSE LEVEL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 290832 | TANDEM T: SLIM INSULIN DELIVERY SYS | INSULIN PUMP | LZG | TANDEM DIABETES | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 59 YR | INSULIN SET| INSULIN: HUMALOG |