Stealth® Spring Clip A1604Recalls & reported problems

Applied Medical Resources Corporation · 3/4 Force Surgical Spring Clip · Class 2

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 00607915113902), received between May 14, 2025 and May 14, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Slipped” (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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Device Slipped1

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.

MalfunctionMay 14, 2025Device Slipped; Device Slipped
TYPE OF PROCEDURE: [AV FISTULA]. EVENT DESCRIPTION: [DURING THE AV FISTULA CREATION, [DOCTOR] APPLIED THE SOFT/SOFT CLIP, TO THE BRACHIAL ARTERY FOR OCCLUSION. HOWEVER, IT SLIPPED OFF DUE TO INSUFFICIENT TRACTION OF THE PAD SURFACE TO THE ARTERY PER HIS FEEDBACK. THE VESSEL WAS NOT DAMAGED. PATIENT IS FINE. [DOCTOR] LIKED THE LATIS/LATIS AND FIBRA OPTIONS HE USED.] PATIENT STATUS: [PATIENT IS FINE]. INTERVENTION: [USAGE OF A CLIP WITH A DIFFERENT PAD, SUCH AS SOFT/FIBRA.]
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22020204 ↗

Device details

UDI-DI	`00607915113902`
Brand	Stealth® Spring Clip
Model	A1604
Company	Applied Medical Resources Corporation
Product code	DSS · Clip, Vascular
Class	Class 2
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	Jun 10, 2022

Device type (GMDN): Surgical bulldog clamp, single-use

A manual surgical instrument designed to grasp, join, compress or support an organ, vessel or soft-tissue. It has a flat, pincer-like design with self-retaining jaws that open upon squeezing of the handles and close upon release; it is typically made of plastic. It is commonly used for vascular clamping and is not dedicated to a specific type of non-vascular surgery. This is a single-use device.

Other Clip, Vascular devices

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Soft/Soft Spring Clip A1801
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Soft/Fibra® Spring Clip G-6050
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All Clip, Vascular devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.