NON-DEHP TUBING W/NON-VENT BAG VENT 0.2 U FLTR, Adverse Event — Malfunction (MDR 1722139-2020-00152)
NON-DEHP TUBING W/NON-VENT BAG VENT 0.2 U FLTR, Adverse Event — Malfunction (MDR 1722139-2020-00152) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NON-DEHP TUBING W/NON-VENT BAG VENT 0.2 U FLTR,; Generic name: INFUSION PUMP AND ACCESSORY SETS; Manufacturer: MOOG MEDICAL DEVICE
| Device | NON-DEHP TUBING W/NON-VENT BAG VENT 0.2 U FLTR, |
|---|---|
| Generic name | INFUSION PUMP AND ACCESSORY SETS |
| Manufacturer | MOOG MEDICAL DEVICES GROUP |
| Report number | 1722139-2020-00152 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | THIS DEVICE WAS NOT RETURNED TO MMDG FOR EVALUATION. A DHR REVIEW WAS COMPLETED AND NO NON-CONFORMANCES WERE FOUND. BECAUSE THE DEVICE WAS NOT RETURNED, NO INVESTIGATION COULD BE PERFORMED AND MMDG IS NOT ABLE TO CONFIRM THE COMPLAINT. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →