Amplatz Goose Neck™ GN1000 (UDI 00763000762360)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000762360), received between Dec 10, 2025 and Dec 10, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

• MalfunctionDec 10, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING A PROCEDURE TO REMOVE AN IVC FILTER VIA RIGHT JUGULAR VEIN ACCESS USING THE GOOSENECK SNARE, THE DISTAL TIP OF THE SNARE CATHETER BROKE OFF WITHIN THE VESSEL. THE BROKEN PORTION OF THE CATHETER WAS UNABLE TO BE RETRIEVED AND WAS LEFT WITHIN THE VESSEL. THE CATHETER AND SNARE WERE REMOVED AS A UNIT, AND A NEW DEVICE WAS USED TO COMPLETE THE PROCEDURE. NO ABNORMALITIES IN ANATOMY, RESISTANCE, OR VESSEL STENOSIS WERE NOTED. THE VESSEL HAD MINIMAL TORTUOSITY AND CALCIFICATION, WITH A DIAMETER OF 21MM. THE INSTRUCTIONS FOR USE WERE FOLLOWED WITHOUT ISSUE. NO PATIENT SYMPTOMS, COMPLICATIONS, ADVERSE OUTCOMES, ILLNESSES, INFECTIONS, OR DEATHS WERE REPORTED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT. THE PIECE OF CATHETER THAT BROKE OFF WILL NOT BE RETRIEVED AT A LATER DATE

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23768445 ↗