AMS 700 CX MS Pump 72404282-10Recalls & reported problems
Boston Scientific Corporation · AMS 700 Inflatable Penile Prosthesis, Preconnected 1 MS Pump to 2 CX Cylinders with 10 cm long preconnect tubing length, Penoscrotal · Class 3 · Implant
All models of AMS 700 CX MS Pump (24)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00878953009834), received between May 2, 2024 and May 7, 2025 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Deflation Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Deflation Problem1
- Mechanical Problem1
- Migration1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 7, 2025Migration; Migration
IT WAS REPORTED THAT THE PATIENT STATED HIS INFLATABLE PENILE PROSTHESIS FELT SIGNIFICANTLY SHORTER COMPARED TO HIS PREVIOUS DEVICE, REPORTING A LOSS OF 2 INCHES IN LENGTH AND HALF AN INCH IN GIRTH. HOWEVER, THE PATIENT SERVICE SPECIALIST CONFIRMED THAT THE CORPORAL MEASUREMENTS, CYLINDER SIZE, AND DEVICE TYPE WERE THE SAME IN BOTH PROCEDURES. THE PATIENT ALSO REPORTED A SENSATION OF THE DEVICE SLIPPING OR DISAPPEARING INTO HIS ABDOMEN. HE STATED HE HAD NOT YET DISCUSSED THESE CONCERNS WITH HIS PHYSICIAN BUT PLANNED TO DO SO, AS HE WISHES TO HAVE THE DEVICE REPLACED. NO ADDITIONAL INFORMATION WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21981434 ↗MalfunctionMay 2, 2024Deflation Problem; Mechanical Problem; Deflation Problem; Mechanical Problem
IT WAS REPORTED THAT UPON PREPARING THE DEVICE, THE SCRUB TECH HAVING DIFFICULTY DEFLATING THE DEVICE. PROPER STEPS WERE TAKEN WHEN PREPARING THE DEVICE AND THE DEVICE INFLATED, BUT WHEN PRESSING THE RELEASE VALVE, NO FLUID WOULD EXIT THE CYLINDERS. THE PHYSICIAN TRIED SEVERAL TROUBLE SHOOTING TECHNIQUES SUCH AS THE HARD RESET AND ALTERNATING BETWEEN THE INFLATE BULB AND DEFLATE BUTTON. AT ONE POINT, WE WERE ABLE TO DEFLATE THE DEVICE, BUT UPON RE-INFLATING, THE SAME ISSUE OCCURRED. THE PHYSICIAN WAS NOT COMFORTABLE IMPLANTING THIS DEVICE, SO AN ALTERNATE DEVICE WAS USED TO COMPLETE THE PROCEDURE. A VALVE ISSUE WITHIN THE PUMP WAS SUSPECTED. THERE WERE NO PATIENT COMPLICATIONS RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19233907 ↗
Other Prosthesis, Penis, Inflatable devices
- AMS 700 MS Pump 72404310Boston Scientific Corporation · Prosthesis, Penis, Inflatable992 reports
- AMS 700 LGX MS Pump 72404252Boston Scientific Corporation · Prosthesis, Penis, Inflatable1 death757 reports
- AMS 700 CX MS Pump 72404233-12Boston Scientific Corporation · Prosthesis, Penis, Inflatable656 reports
- AMS 700 CX MS Pump 72404232Boston Scientific Corporation · Prosthesis, Penis, Inflatable639 reports
- AMS 700 LGX MS Pump 72404251Boston Scientific Corporation · Prosthesis, Penis, Inflatable611 reports
- Conceal 720185-01Boston Scientific Corporation · Prosthesis, Penis, Inflatable586 reports
- AMS 700 LGX MS Pump 72404252-10Boston Scientific Corporation · Prosthesis, Penis, Inflatable561 reports
- AMS 700 CX MS Pump 72404232-10Boston Scientific Corporation · Prosthesis, Penis, Inflatable533 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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