AMPLATZ GOOSE NECK™ GN3000Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000225308), received between Jun 16, 2021 and Jun 16, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

1 other recall cover devices cleared under the same FDA submission (K972511); they may or may not involve this specific model.

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 16, 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.

• InjuryJun 16, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

  PHYSICIAN ATTEMPTED TO USE A GOOSENECK SNARE DURING TREATMENT IN THE PATIENT¿S LEFT ILIAC VEIN. THE DEVICE WAS INSPECTED WITHOUT ISSUES IDENTIFIED. IFU WAS FOLLOWED DURING PREPARATION. IT IS REPORTED A RADIOPAQUE MARKER WAS OBSERVED IN THE PATIENT¿S ILIAC VEIN POST REMOVAL OF THE DEVICE. A CATHETER WAS USED TO ASPIRATE, AND THE MARKER WAS REMOVED WITH ROUGHLY 50 ML OF BLOOD. NO FURTHER INJURY REPORTED.

  Patient problems: Unspecified Tissue Injury

  MAUDE report 12007000 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K972511. One submission often covers many models, so check the product and lot details in each record.

• Z-0992-2007 · May 18, 2007 · Terminated
  Amplatz Goose Neck Snare Kit, 6 Fr, Lot 1650307, REF: GN3000, Use By 2009-09-01, Sterile EO ev3 4600 Nathan Lane North, Plymouth, MN 55442-2920 USA THE ENDOVASCULAR COMPANY. The