FDA Adverse Event
Malfunction
Summary report: N
BELT CLIP
MDR report key: 4120031
·
Received September 25, 2014
Report
- Report Number
- 2032227-2014-28528
- Event Type
- Malfunction
- Date Received
- September 25, 2014
- Date of Event
- June 28, 2014
- Report Date
- August 28, 2014
- Manufacturer
- MEDTRONIC MINIMED
- Product Code
- MDS
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY
- Reporter Occupation
- PATIENT
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 THAT THE INSULIN PUMP WAS BROKEN. THE CUSTOMER'S BLOOD GLUCOSE WAS UNKNOWN. NOTHING FURTHER WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 597870 | BELT CLIP | CGM | MDS | MEDTRONIC MINIMED | MMT-640 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 69 YR |