Latis® Spring Clip A1611Recalls & reported problems

Applied Medical Resources Corporation · 1/2 Force Surgical Spring Clip · Class 2

Data updated Oct 16, 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 00607915110598), received between Sep 22, 2022 and Sep 22, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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 16, 2026.

Most reported problems

Device problems

Break1

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.

MalfunctionSep 22, 2022Break; Break
PROCEDURE PERFORMED: CABG. EVENT DESCRIPTION: WHEN TRYING TO PUT A CLAMP ON THE IMA THE CLAMP BROKE. ALL PIECES WERE REMOVED FROM THE PATIENT, THERE WAS NO PATIENT INJURY. IT IS UNKNOWN HOW THE CASE WAS COMPLETED. THE EVENT UNIT IS NOT RETURNING. THE REMAINING STERILE UNITS FROM THE SAME BOX WILL BE RETURNING. ADDITIONAL INFORMATION WAS RECEIVED VIA EMAIL ON (B)(6) 2022 FROM HEALTH SYSTEM MANAGER REP HAS BEEN UNABLE TO GET ANY INFORMATION. REP SHOULD BE ABLE TO FIND OUT HOW MANY PRODUCTS WILL BE RETURNED. ADDITIONAL INFORMATION WAS RECEIVED VIA EMAIL ON (B)(6) 2022 FROM HEALTH SYSTEM MANAGER THERE ARE (B)(4) STERILE UNITS BEING RETURNED. PATIENT STATUS: NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15463279 ↗

Device details

UDI-DI	`00607915110598`
Brand	Latis® Spring Clip
Model	A1611
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/Fibra® Spring Clip G-6050
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Stealth® Spring Clip A1604
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1 report
Soft/Soft Spring Clip A1801
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Sof/Soft Spring Clip G-1200
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All Clip, Vascular devices →

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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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