MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION AMS 700 Spherical Reservoir; prosthesis, penis, inflatable

Model Number	72404156
Medical Device Problem Code	Migration (4003)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/13/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the patient implanted with this inflatable penile prosthesis (ipp) was dissatisfied because the reservoir tubing was palpable.A surgical revision procedure was performed, during which no device issue was identified, and the device was confirmed to be functioning as intended.However, the reservoir was removed and repositioned, with the tubing placed in a deeper location.No additional information was reported.
Additional Manufacturer Narrative
Concomitant products implanted at time of event: model number/catalog number: 72404232-10.Serial number: n/a.Batch/lot number: 1100466366.Model/catalog description: cx preconnect ms 18cm ps 10cm tl iz.Unique identifier (udi): (b)(4).Model number/catalog number: 72404156.Serial number: n/a.Batch/lot number: 1100518472.Model/catalog description: reservoir 100 ml pc/iz.Unique identifier (udi): (b)(4).

• Brand Name: AMS 700 Spherical Reservoir
• 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: 50209651
• Report Number: 2124215-2026-42919
• Device Sequence Number: 10019045
• Product Code: JCW
• UDI-Device Identifier: 00878953003214
• UDI-Public: (01)00878953003214(17)260523(10)1100518472
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• PMA/510(K) Number: N970012
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Device Explanted Year: 2026
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 08/11/2026

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: 05/23/2026
• Device Model Number: 72404156
• Device Catalogue Number: 72404156
• Device Lot Number: 1100518472
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 07/29/2026
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/13/2026
• Initial Report FDA Received Date: 08/11/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 05/23/2024
• 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
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 63 YR
• Patient Sex: Male