PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR Adverse Event — Injury (MDR 2032227-2008-00371)
PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR Adverse Event — Injury (MDR 2032227-2008-00371) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR; Generic name: INFUSION PUMP; Manufacturer: MEDTRONIC MINIMED.
| Device | PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR |
|---|---|
| Generic name | INFUSION PUMP |
| Manufacturer | MEDTRONIC MINIMED |
| Report number | 2032227-2008-00371 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-21 |
| Report source | Consumer |
| Narrative | THE CUSTOMER STATED, THAT SHE WAS HOSPITALIZED DUE TO HYPERGLYCEMIA. THE BLOOD GLUCOSE READING AT THE TIME OF HOSPITALIZATION WAS NOT REPORTED. THE CUSTOMER STATED, THAT TWO DAYS PRIOR TO THE EVENT, SHE WAS VOMITING AND TOOK OFF THE INSULIN PUMP. THE CUSTOMER STATED, THAT SHE MIGHT HAVE HAD FOOD POISONING. THE CUSTOMER STATED, THAT PRIOR TO THE EVENT, SHE STARTED USING THE INSULIN PUMP AGAIN. TROU |
| Source | openFDA MAUDE (device adverse events) |
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