FDA Adverse Event
Injury
Summary report: N
BELT CLIP PUMP CLEAR
MDR report key: 4233449
·
Received November 6, 2014
Report
- Report Number
- 2032227-2014-48864
- Event Type
- Injury
- Date Received
- November 6, 2014
- Date of Event
- September 1, 2014
- Report Date
- October 9, 2014
- Manufacturer
- MEDTRONIC MINIMED
- Product Code
- OYC
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
CURRENTLY IT IS UNKNOWN WHETHER OR NOT THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT AS NO PRODUCT HAS BEEN RETURNED. NO CONCLUSION CAN BE DRAWN AT THIS TIME. WE THEREFORE CONSIDER THIS REPORT COMPLETE TO THE BEST OF OUR KNOWLEDGE.
Description of Event or Problem · 1
IT WAS REPORTED THE CUSTOMER WAS IN THE EMERGENCY ROOM FOR A MENTAL BREAKDOWN. THE CUSTOMER ALSO STATED SHE WAS UNABLE TO LOCATE HER BELT CLIP. NO ADDITIONAL INFORMATION PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 712752 | BELT CLIP PUMP CLEAR | INSULIN INFUSION PUMP / SENSOR AUGMENTED | OYC | MEDTRONIC MINIMED | MMT-631CL |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 51 YR | Hospitalization |