NAMIC 650107522Recalls & 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: 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 H9656501075220), received between Nov 14, 2017 and Nov 14, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Uncoiled” (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

Uncoiled1

Patient problems

No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

MalfunctionNov 14, 2017Uncoiled; Uncoiled
AS REPORTED, UPON REMOVING THE GUIDEWIRE FROM THE PATIENT, IT WAS NOTED THAT THE GUIDEWIRE HAD BECOME UNRAVELLED. THE GUIDEWIRE HAD BEEN PROVIDED IN A CONVENIENCE KIT SOLD ON A NON-STERILE BASIS BY ANGIODYNAMICS TO CARDINAL HEALTH FOR INCLUSION ON A TRAY PACK. THERE WAS NO NEGATIVE PATIENT IMPACT FROM THIS EVENT. IT HAS BEEN INDICATED THAT THE USED GUIDEWIRE WILL BE RETURNED TO ANGIODYNAMICS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7027319 ↗

Device details

UDI-DI	`H9656501075220`
Brand	NAMIC
Model	650107522
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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