FDA Adverse Event
Malfunction
Summary report: N
BELT CLIP
MDR report key: 3981941
·
Received August 5, 2014
Report
- Report Number
- 2032227-2014-05273
- Event Type
- Malfunction
- Date Received
- August 5, 2014
- Date of Event
- July 2, 2014
- Report Date
- July 2, 2014
- Manufacturer
- MEDTRONIC MINIMED
- Product Code
- OYC
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MI
- 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 BY THE CUSTOMER THAT THEIR INSULIN PUMP'S BELT CLIP HAD BROKEN. CUSTOMER ALSO STATED THEY WOKE UP IN THE MORNING WITH A BLOOD GLUCOSE LEVEL OF 40 MG/DL DUE TO OVERCORRECTING AFTER EATING A SNACK. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 92 MG/DL AT TIME OF REPORTING. NOTHING FURTHER REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 457576 | BELT CLIP | INSULIN INFUSION PUMP / SENSOR AUGMENTED | OYC | MEDTRONIC MINIMED | MMT-642 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 46 YR |