MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-29 for UROLIFT manufactured by Neotract, Inc..
[146691024]
Pt had urolift prostate implant - now needing surgery for pain and bleeding and will need surgery for implant removal - stone formed on pt in urethra. Fda safety report id# (b)(4).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5087009 |
| MDR Report Key | 8655449 |
| Date Received | 2019-05-29 |
| Date of Report | 2019-05-24 |
| Date of Event | 2019-05-24 |
| Date Added to Maude | 2019-05-30 |
| 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 | UROLIFT |
| Generic Name | IMPLANTABLE TRANSPROSTATIC TISSUE RETRACTOR SYSTEM |
| Product Code | PEW |
| Date Received | 2019-05-29 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | NEOTRACT, INC. |
| Manufacturer Address | US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2019-05-29 |