AMPLATZ GOOSE NECK SK201Recalls & reported problems
Covidien LP · Microsnare Kit · Class 2
All models of AMPLATZ GOOSE NECK (10)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00821684005040), received between Jun 23, 2021 and Jun 23, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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
Device problems
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 23, 2021Fracture; Fracture
PHYSICIAN WAS ATTEMPTED TO USE A MICRO SNARE DEVICE DURING PROCEDURE. IT WAS REPORTED THAT THE CATHETER WAS BROKEN DURING THE PROCEDURE. THE CATHETER WAS FRACTURED. THE DEVICE DID ENTER PATIENT. NO COMPONENT OF THE DEVICE DETACHED IN THE PATIENT ANATOMY, AND NO INTERVENTION WAS REQUIRED FOR REMOVAL. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12047603 ↗
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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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