MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-02-27 for IMPELLA 2.5 PUMP IMPELLA 2.5 PUMP SET, JAPAN 005048-JP manufactured by Abiomed, Inc..
[182038242]
Product has not been returned; investigation has not been completed.
Patient Sequence No: 1, Text Type: N, H10
[182038243]
The complainant reported a (b)(6) japanese female patient had impella 2. 5 pump inserted in the left femoral for high risk percutaneous coronary interventions (hrpci). It was reported the physician suspected hemolysis one hour after impella was implanted. Impella? S position was adjusted in order to resolve the issue; however, this was unsuccessful. Continuous hemofiltration/hemodiafiltration (chdf) was performed and the device was explanted due to the hemolysis. No further information was provided.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1220648-2020-00356 |
| MDR Report Key | 9765841 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2020-02-27 |
| Date of Report | 2020-02-27 |
| Date of Event | 2020-01-29 |
| Date Facility Aware | 2020-01-29 |
| Date Mfgr Received | 2020-01-29 |
| Device Manufacturer Date | 2019-04-16 |
| Date Added to Maude | 2020-02-27 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. RALPH BARISANO |
| Manufacturer Street | 22 CHERRY HILL DR |
| Manufacturer City | DANVERS MA 01923 |
| Manufacturer Country | US |
| Manufacturer Postal | 01923 |
| Manufacturer G1 | ABIOMED EUROPE GMBH |
| Manufacturer Street | NEUENHOFER WEG 3 |
| Manufacturer City | AACHEN 52074 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 52074 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | IMPELLA 2.5 PUMP |
| Generic Name | TEMPORARY NON-ROLLER TYPE LEFT HEART SUPPORT BLOOD PUMP |
| Product Code | OZD |
| Date Received | 2020-02-27 |
| Model Number | IMPELLA 2.5 PUMP SET, JAPAN |
| Catalog Number | 005048-JP |
| Lot Number | 1406291 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ABIOMED, INC. |
| Manufacturer Address | 22 CHERRY HILL DR DANVERS MA 01923 US 01923 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2020-02-27 |