MINILOC SAFETY INFUSION SET 20G X 0.75IN Adverse Event — Malfunction (MDR 3006260740-2020-01531)
MINILOC SAFETY INFUSION SET 20G X 0.75IN Adverse Event — Malfunction (MDR 3006260740-2020-01531) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MINILOC SAFETY INFUSION SET 20G X 0.75IN; Generic name: SET, ADMINISTRATION, INTRAVASCULAR; Manufacturer: BARD ACCESS SYSTEMS.
| Device | MINILOC SAFETY INFUSION SET 20G X 0.75IN |
|---|---|
| Generic name | SET, ADMINISTRATION, INTRAVASCULAR |
| Manufacturer | BARD ACCESS SYSTEMS |
| Report number | 3006260740-2020-01531 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, USER F |
| Narrative | THE DEVICE HAS NOT BEEN RETURNED TO THE MANUFACTURER FOR EVALUATION. A LOT HISTORY REVIEW (LHR) OF ASDUF029 SHOWED NO OTHER SIMILAR PRODUCT COMPLAINT(S) FROM THIS LOT NUMBER. |
| Source | openFDA MAUDE (device adverse events) |
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