FDA Adverse Event
Injury
Summary report: N
TANDEM T: SLIM INSULIN DELIVERY SYSTEM
MDR report key: 3931630
·
Received June 24, 2014
Report
- Report Number
- 3007981285-2014-01459
- 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
- Report Source
- Manufacturer report
- Reporter Location
- MS, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
NO PRODUCT RETURNING FOR EVAL. ATTEMPTS HAVE BEEN MADE TO OBTAIN ALL EVENT INFO. SHOULD NEW INFO BECOME AVAILABLE, A F/U MDR WILL BE SUBMITTED.
Description of Event or Problem · 1
RECEIVED INFO STATING THAT DUE TO USER ERROR, CUSTOMER DELIVERED A BOLUS OF 13 UNITS OF INSULIN. REPORTEDLY, THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 368935 | TANDEM T: SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES CARE INC. | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 39 YR | Other |