NAMIC 651800217Recalls & reported problems

Navilyst Medical, Inc. · NAMIC Convenience Kit

All models of NAMIC (41)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 1
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI H9656518002170), received between Jun 30, 2017 and Jun 30, 2017 — classified as 1 death.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

Insufficient Device Problem Information1

Patient problems

Air Embolism1
Sudden Cardiac Death1

Recent adverse event reports

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

DeathJun 30, 2017Insufficient Device Problem Information; Insufficient Device Problem Information
AS REPORTED, AIR WAS INJECTED INTO THE PATIENT DURING A CARDIAC ANGIOGRAM PROCEDURE UTILIZING AN ANGIODYNAMICS CONVENIENCE KIT. MANIFOLD WAS PREPARED IN USUAL FASHION, CONNECTIONS CHECKED AND ALL WERE SECURE. CONTRAST WAS PRIMED. AFTER TIG CATHETER INSERTION WAS CONNECTED BY MD BOTH CATHETER AND MANIFOLD FLUSHED. TWO PICTURES WERE TAKEN AND ON THE THIRD PICTURE IT WAS NOTED THAT THERE WAS AIR EMBOLI IN THE CIRCUMFLEX. PATIENT DECOMPENSATED, CODED AND DIED AFTER PROLONGED RESUSCITATION. THE USED COMPONENTS HAVE BEEN PROVIDED TO A 3RD PARTY HIRED BY THE HOSPITAL TO INVESTIGATE THE ROOT CAUSE OF THE EVENT.
Patient problems: Air Embolism; Sudden Cardiac Death
MAUDE report 6680293 ↗

Device details

UDI-DI	`H9656518002170`
Brand	NAMIC
Model	651800217
Company	Navilyst Medical, Inc.
Product code	—
Class	—
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Mar 29, 2018

Device type (GMDN): Angiography kit

A collection of sterile devices and equipment used to prepare a patient for the radiographic visualization of the arteries of a particular organ system or body part through the vascular injection of contrast media. It typically includes a combination of fluid/contrast media administration devices (e.g., tubing, manifold, stopcocks, and syringes) and/or dedicated angiography supportive devices (e.g., angiography drapes, covers, dressings); the angiography catheter is not included. This is a single-use device.

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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