MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-01-02 for SWITCHPOINT INFINITY 3 067800/000 manufactured by Stryker Corp..
[96365137]
Laparoscopic equipment. Battery changed. Functioned properly briefly. Lap monitors shut down.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5074376 |
| MDR Report Key | 7159824 |
| Date Received | 2018-01-02 |
| Date of Report | 2017-12-28 |
| Date of Event | 2017-06-14 |
| Date Added to Maude | 2018-01-03 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| 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 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | SWITCHPOINT INFINITY 3 |
| Generic Name | ROUTER/SWITCH/HUB |
| Product Code | OCS |
| Date Received | 2018-01-02 |
| Model Number | 067800/000 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER CORP. |
| Manufacturer Address | WASHINGTON DC US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2018-01-02 |