FDA Adverse Event
Injury
Summary report: N
TANDEM T:SLIM INSULIN DELIVER PUMP
MDR report key: 3893939
·
Received June 12, 2014
Report
- Report Number
- 3007981285-2014-01108
- Event Type
- Injury
- Date Received
- June 12, 2014
- Date of Event
- May 13, 2014
- Report Date
- May 15, 2014
- Manufacturer
- TANDEM DIABETES
- Product Code
- LZG
- PMA / PMN Number
- K111210
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- 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. USE OF APIDRA INSULIN IS CONTRAINDICATED FOR THE T:SLIM CARTRIDGE.
Description of Event or Problem · 1
RECEIVED INFO STATING CUSTOMER RECEIVED MULTIPLE OCCLUSION ALARMS. REPORTEDLY, THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IMPACTED. THE CUSTOMER WAS USING APIDRA INSULIN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 348684 | TANDEM T:SLIM INSULIN DELIVER PUMP | INSULIN PUMP | LZG | TANDEM DIABETES | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 14 YR | Other | APIDRA |