CONMED 270179Recalls & reported problems

Conmed Corporation · Infuser Compressor 110V 60 Hz · Class 2

Data updated Oct 13, 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 30653405048026), received between Jul 25, 2025 and Jul 25, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unintended Electrical Shock” (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

Unintended Electrical Shock1

Patient problems

Electric Shock1

Recent adverse event reports

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

MalfunctionJul 25, 2025Unintended Electrical Shock; Unintended Electrical Shock
A SALES REPRESENTATIVE REPORTED ON BEHALF OF A CUSTOMER THAT THE 270179, INFUSER COMPRESSOR 110V 60 HZ DEVICE WAS USED IN AN UNNAMED PROCEDURE ON APPROXIMATELY ON (B)(6) 2025, AND ¿CAP TO FUSE BROKE OFF CAUSING IT TO LIGHTLY SHOCK PEOPLE (EVERYONE'S OKAY)¿. THROUGH FOLLOW-UP ASSESSMENT, THE CUSTOMER "CONFIRMED IT WAS ONLY ONE PERSON WHO GOT SHOCKED. THEY PULLED THE EQUIPMENT OUT OF THE OR RIGHT AFTER THE CASE AND IT WASN'T USED AGAIN.". THERE WAS NO REPORT OF INJURY, MEDICAL/SURGICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR THE PATIENT OR USER. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: Electric Shock
MAUDE report 22609997 ↗

Device details

UDI-DI	`30653405048026`
Brand	CONMED
Model	270179
Company	Conmed Corporation
Product code	FRN · Pump, infusion
Class	Class 2
FDA submission	K990447
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Aug 14, 2024

Device type (GMDN): Intravenous pressure infusor, automated

A pneumatically-powered device designed to increase the rate of an intravenous (IV) infusion given to a patient by applying pressure directly to the infusion bag. The device is designed with a pressure chamber into which the infusion bag is secured, and is connected to a supply of pressurized air which, when activated, creates pressure in the rear of the chamber. It typically includes a pressure gauge to indicate the applied pressure and overpressure safety features.

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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 13, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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