KIT MMT-1761WWK 670G V4.11 SF MG Adverse Event — Malfunction (MDR 2032227-2020-111044)
KIT MMT-1761WWK 670G V4.11 SF MG Adverse Event — Malfunction (MDR 2032227-2020-111044) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: KIT MMT-1761WWK 670G V4.11 SF MG; Generic name: ARTIFICIAL PANCREAS DEVICE SYSTEM, SINGLE HORMONAL CONTROL; Manufacturer: MEDTRONIC PUERTO RICO
| Device | KIT MMT-1761WWK 670G V4.11 SF MG |
|---|---|
| Generic name | ARTIFICIAL PANCREAS DEVICE SYSTEM, SINGLE HORMONAL CONTROL |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 2032227-2020-111044 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | Foreign, Company representation |
| Narrative | (B)(4). 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. |
| Source | openFDA MAUDE (device adverse events) |
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