FDA Adverse Event
Injury
Summary report: N
TANDEM T: SLIM INSULIN DELIVERY SYSTEM
MDR report key: 3935483
·
Received June 23, 2014
Report
- Report Number
- 3007981285-2014-01297
- Event Type
- Injury
- Date Received
- June 23, 2014
- Date of Event
- May 22, 2014
- Report Date
- May 23, 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
- TN, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
THE DEVICE IS AVAILABLE FOR EVALUATION; HOWEVER, THE DEVICE HAS NOT BEEN RECEIVED FOR EVALUATION. A FOLLOW UP MDR WILL BE FILED IF THE DEVICE IS RECEIVED.
Description of Event or Problem · 1
RECEIVED INFORMATION STATING CUSTOMER'S FILL ESTIMATE WAS INACCURATE. REPORTEDLY, CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 367065 | TANDEM T: SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES CARE INC. | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 53 YR | Other |