MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-03-30 for AMS INFLATABLE PENILE PROSTHESIS 72404014 manufactured by Boston Scientific Corporation.
[187567435]
It was reported that the patient underwent a revision procedure due to cylinder micro puncture with an inflatable penile prosthesis (ipp). The ipp cylinder, pump, and reservoir was explanted and a new ipp cylinder, pump, and balloon was implanted. During the revision procedure was tested and found saline leaks in the cylinders. The patient recovered following the procedure.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2183959-2020-01707 |
MDR Report Key | 9900594 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2020-03-30 |
Date of Report | 2020-03-30 |
Date of Event | 2020-03-09 |
Date Mfgr Received | 2020-03-09 |
Device Manufacturer Date | 2012-08-20 |
Date Added to Maude | 2020-03-30 |
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 | 4089353452 |
Manufacturer G1 | BOSTON SCIENTIFIC 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 INFLATABLE PENILE PROSTHESIS |
Generic Name | DEVICE IMPOTENCE MECHANICAL/HYDRAULIC |
Product Code | FHW |
Date Received | 2020-03-30 |
Model Number | 72404014 |
Catalog Number | 72404014 |
Lot Number | 785455001 |
Device Expiration Date | 2017-08-01 |
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 | 2020-03-30 |