LAP-BAND® AP System Standard with RapidPort® EZ C-2360Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00850007764609), received between Apr 19, 2023 and Apr 19, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 19, 2023Fluid/Blood Leak; Fluid/Blood Leak

  SURGEON REPORTED TO SALES REPRESENTATIVE THAT HE SUSPECTS A LEAK IN A LAP-BAND SYSTEM THAT HE IMPLANTED. HE HAS EXAMINED THE PORT AND PORT TUBING AND DID NOT OBSERVE A LEAK. HE SUSPECTS THE LEAK IS IN THE BAND TUBING OR THE BAND ITSELF.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 16773828 ↗