MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-24 for AMS SPECTRA CONCEALABLE PENILE PROSTHESIS UNK-P-SPP manufactured by Boston Scientific Corporation.
        [186104870]
It was reported that the patient underwent a spectra penile prosthesis (spp) revision surgery due to unspecified reasons. During the procedure the existing device was removed and a new inflatable penile prosthesis (ipp) was implanted. No information was provided about the patient's outcome.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2183959-2020-01575 | 
| MDR Report Key | 9875979 | 
| Report Source | HEALTH PROFESSIONAL | 
| Date Received | 2020-03-24 | 
| Date of Report | 2020-03-24 | 
| Date of Event | 2020-03-04 | 
| Date Mfgr Received | 2020-03-04 | 
| Date Added to Maude | 2020-03-24 | 
| 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 | ALYSON HARRIS | 
| Manufacturer Street | 10700 BREN ROAD W | 
| Manufacturer City | MINNETONKA MN 55343 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 55343 | 
| Manufacturer Phone | 4083953452 | 
| Manufacturer G1 | BOSTON SCEINTIFIC CORPORATION | 
| Manufacturer Street | 10700 BREN ROAD W | 
| Manufacturer City | MINNETONKA MN 55343 | 
| Manufacturer Country | US | 
| Manufacturer Postal Code | 55343 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | AMS SPECTRA CONCEALABLE PENILE PROSTHESIS | 
| Generic Name | PROSTHESIS PENILE | 
| Product Code | FAE | 
| Date Received | 2020-03-24 | 
| Model Number | UNK-P-SPP | 
| Catalog Number | UNK-P-SPP | 
| Operator | LAY USER/PATIENT | 
| Device Availability | N | 
| Device Eval'ed by Mfgr | R | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | BOSTON SCIENTIFIC CORPORATION | 
| Manufacturer Address | 10700 BREN ROAD W MINNETONKA MN 55343 US 55343 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2020-03-24 |