MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION AMS 700 CXR; PROSTHESIS, PENIS, INFLATABLE

Model Number	72404011
Medical Device Problem Codes	Mechanical Problem (1384); Material Puncture/Hole (1504); Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/07/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that this inflatable penile prosthesis was not working properly.Two weeks later, a surgical procedure was performed, during which a crack in the left cylinder connecting tube was noted.All components were removed and replaced.No patient complications were reported.
Additional Manufacturer Narrative
Pump unique identifier (udi) # (b)(4).Reservoir unique identifier (udi) # (b)(4).
Additional Manufacturer Narrative
Upon receipt at our quality assurance laboratory, this inflatable penile prosthesis (ipp) underwent a thorough analysis.Both cylinders were microscopically inspected and leak tested.The proximal end of the first cylinder presented a leak and a hole, along with broken fabric threads, and a spiraling detachment of its outer tube.The second cylinder exhibited wear at fold in its middle portion, but no leaks were identified.The pump was microscopically inspected, leak and functionally tested.While its kink resistant tubing (krt) was worn to the filament, the component passed leakage and functional evaluation.The reservoir was microscopically inspected and tested for leaks.Wear at fold in its shell was noted, but no leaks were identified.Based on the information available and analysis results, the leak found in the first cylinder could have caused or contributed to the reported clinical observations.Pump unique identifier (udi) # (b)(4).Reservoir unique identifier (udi) # (b)(4).
Event or Problem Description
It was reported that this inflatable penile prosthesis was not working properly.Two weeks later, a surgical procedure was performed, during which a crack in the left cylinder connecting tube was noted.All components were removed and replaced.No patient complications were reported.

• Brand Name: AMS 700 CXR
• Common Device Name: PROSTHESIS, PENIS, INFLATABLE
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer Contact: farshad fahimi ; 4100 hamline avenue north; building c; saint paul, MN 55112
• MDR Report Key: 21785408
• Report Number: 2124215-2025-20867
• Device Sequence Number: 8676218
• Product Code: JCW
• UDI-Device Identifier: 00878953002682
• UDI-Public: (01)00878953002682(17)230121(10)1000039182
• Combination Product (Y/N): N
• Initial Reporter Country: KS
• PMA/510(K) Number: N970012
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2025
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 06/02/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Expiration Date: 01/21/2023
• Device Model Number: 72404011
• Device Catalogue Number: 72404011
• Device Lot Number: 1000039182
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/24/2025
• Supplement Date Received by Manufacturer: 05/28/2025
• Initial Report FDA Received Date: 04/07/2025
• Supplement Report FDA Received Date: 06/02/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/22/2018
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: PUMP: UPN: 72404310 / LOT: 1000509331; PUMP: UPN: 72404310 / LOT: 1000509331; RESERVOIR: UPN: 72404161 / LOT: 1000539514; RESERVOIR: UPN: 72404161 / LOT: 1000539514
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 63 YR
• Patient Sex: Male