FDA Adverse Event
Injury
Summary report: N
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
MDR report key: 3961550
·
Received June 16, 2014
Report
- Report Number
- 3007981285-2014-03234
- Event Type
- Injury
- Date Received
- June 16, 2014
- Date of Event
- June 18, 2014
- Report Date
- June 20, 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
- FL, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
NO PRODUCT RETURNING FOR EVALUATION. SHOULD NEW INFORMATION BECOME AVAILABLE, A FOLLOW UP REPORT WILL BE SUBMITTED. USE OF APIDRA INSULIN IS CONTRAINDICATED FOR THE T:SLIM CARTRIDGE.
Description of Event or Problem · 1
RECEIVED INFORMATION STATING CUSTOMER RECEIVED MULTIPLE OCCLUSION ALARMS. REPORTEDLY CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED. CUSTOMER WAS USING APIDRA INSULIN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 351969 | TANDEM T:SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES CARE INC. | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 29 YR | Other | INSULIN: APIDRA |