MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-07-24 for AV400 AV 400 manufactured by Accuvein, Inc..
[114837950]
This was a malfunction of the accuvein device where the screen had only showed a partial display. We have seen these issues in the past, but the return and replace policy of accuvein has allowed for timely resolution to issues.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 7713508 |
| MDR Report Key | 7713508 |
| Date Received | 2018-07-24 |
| Date of Report | 2018-07-20 |
| Date of Event | 2018-07-11 |
| Report Date | 2018-07-20 |
| Date Reported to FDA | 2018-07-20 |
| Date Reported to Mfgr | 2018-07-24 |
| Date Added to Maude | 2018-07-24 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | BIOMEDICAL ENGINEER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | AV400 |
| Generic Name | DEVICE, VEIN LOCATION, LIQUID CRYSTAL |
| Product Code | KZA |
| Date Received | 2018-07-24 |
| Returned To Mfg | 2018-07-16 |
| Model Number | AV 400 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | 1 YR |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ACCUVEIN, INC. |
| Manufacturer Address | 40 GOOSE HILL ROAD COLD SPRING HARBOR NY 11724 US 11724 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-07-24 |