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Atrium Medical Corporation

Atrium Medical Corporation Recalls

All product recalls associated with Atrium Medical Corporation.

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 3661–3680 of 4099 recalls

Atrium Medical Corporation: HydraGlide Heparin Coated Silicone Thoracic Catheters - S...

Heparin-coated Thoracic Catheters were manufactured with heparin allegedly contaminated with oversulfated chondroitin sulfate

FDAMay 12, 2008Nationwide• Atrium Medical Corporation

Atrium Medical Corporation: HydraGlide XL Heparin Coated Silicone Thoracic Catheters,...

Heparin-coated Thoracic Catheters were manufactured with heparin allegedly contaminated with oversulfated chondroitin sulfate

FDAMay 12, 2008Nationwide• Atrium Medical Corporation

GE Healthcare Integrated IT Solutions: GE Centricity AW Suite 2.0 Software running on the Centri...

Incorrect measurement of the aortic length in certain cases of aneurysm during the use of the aorta protocol or customized protocol of the Centricity AW Suite 2.0 running on the Centricity RA 1000 or RA600/CA1000 workstations.

1...182 183184185 186...205

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FDAMay 9, 2008Nationwide• GE Healthcare Integrated IT Solutions

SagaTech Electronics, Inc.: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sle...

The outer jacket is receding away from the black sensor prematurely.

Class IIModerate

FDAMay 8, 2008Nationwide• SagaTech Electronics, Inc.

SagaTech Electronics, Inc.: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sle...

The outer jacket is receding away from the black sensor prematurely.

FDAMay 8, 2008Nationwide• SagaTech Electronics, Inc.

Medtronic International Trade Inc: Medtronic Trillium AFFINITY NT, 511T, Hollow Fiber Oxygen...

Medtronic is advising that certain Trillium-coated Medtronic cardiopulmonary bypass (CBP) products (e.g., oxygenators, reservoirs, pumps and tubing packs) were manufactured with heparin batches contaminated with oversulfated chondroitin sulfate (OSCS). Based upon currently available information, Medtronic has determined that Medtronic Trillium-coated products can continue to be used in cardiopulm

FDAMay 7, 2008Nationwide• Medtronic International Trade Inc

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation; for diagnostic ima...

A software anomaly results in incorrect study date and time information being displayed in the report screen and title, which may result in a potential patient misdiagnosis.

FDAMay 6, 2008Nationwide• GE Healthcare Integrated IT Solutions

Datex Ohmeda, Inc. dba GE Healthcare: Corometrics MODEL 250 Series Maternal/ Fetal Monitor, Mod...

Communication connector within monitor is defective and may cause potential loss of telemetry.

FDAMay 5, 2008Nationwide• Datex Ohmeda, Inc. dba GE Healthcare

Fisher LP Gas Regulators – Leak Hazard (2008)

Fire/Burn Risk

The recalled gas regulators were manufactured from June 2006 through January 2008 and installed on LP-gas supply systems in homes and small commercial buildings. The recall involves model R622H LP-gas regulators with type numbers in the table below: R622H-BGJ R622H-DGJ R622H-HGJ R622H-JGJ R622H-BGK R622H-DGK R622H-HGK R622H-JGK The type number is located on a white label attached to the spring case chimney (see photo). The box label also includes the type number. There are no serial numbers on these regulators. The regulators are date stamped with the month and year (12-07 indicating made in December 2007) of manufacture on the product.

CPSCApr 24, 2008Nationwide• Fisher Controls International (FCI), of McKinney, Texas

Sunquest Information Systems, Inc.: Sunquest Laboratory versions 5.3, 5.4, 6.1, 6.2 and 6.3. ...

Sunquest has identified a problem with IGO interfaces when performing an Online File Cleanup (OFC) that can lead to the test results of one patient filing to another patient when the order codes are the same. Performing an OFC prior to all results being assigned an accession number may cause the patient results to remain in a temporary file where they can be incorrectly associated to the wrong pat

FDAApr 17, 2008Nationwide• Sunquest Information Systems, Inc.

Tri-State Hospital Supply Corporation: Tri-State Hospital Supply Corp., Tri-State Centurion Veno...

The kits contain Monoject prefill heparin lock flush syringes, which were recalled by the manufacturer due to contamination.

FDAApr 8, 2008IN, MS, OH +1 more• Tri-State Hospital Supply Corporation

Gas Water Heaters (A.O. Smith) – Fire Hazard (2008)

Fire/Burn Risk

This recall involves 75-gallon natural and propane gas water heaters. "A.O. Smith" or "State" is printed on the side of the unit. A.O. Smith and State model and serial numbers included in this recall are listed in the chart below. Model and serial numbers are printed on the water heater's rating plate. Brand Name Model Number A.O. Smith FCG-75 300 Serial Number Ranges L07A071460 through L07A144966 or M07A009387 through M07A072884 FCG-75 301 State GS6 75 XRR S GS6 75 CRR S

CPSCApr 3, 2008Nationwide• A.O. Smith Water Products Co., of Ashland City, Tenn.

Abbott Diagnostic International, Ltd. Carr # 2 Km 58.0 Cruce Davila: AxSYM Ultrasensitive hTSH II Master Calibrators Micropar...

High Control value out of range after calibration. --AN INCREASED FREQUENCY OF HIGH CONTROL VALUES BEYOND THE UPPER LIMIT OF THE RANGE SPECIFIED BY THE PACKAGE INSERT.

FDAMar 6, 2008AZ, CA, CO +32 more• Abbott Diagnostic International, Ltd. Carr # 2 Km 58.0 Cruce Davila

Chattanooga Corp Inc: INTELECT LEGEND XT, electromechanical therapeutic ultraso...

Device may fail to administer therapy during use.

FDAFeb 28, 2008Nationwide• Chattanooga Corp Inc

Chattanooga Corp Inc: VECTRA GENISYS, electromechanical therapeutic ultrasound ...

Device may fail to administer therapy during use.

FDAFeb 28, 2008Nationwide• Chattanooga Corp Inc

Chattanooga Corp Inc: INTELECT TRANSPORT ULTRASOUND, electromechanical therapeu...

Device may fail to administer therapy during use.

FDAFeb 28, 2008Nationwide• Chattanooga Corp Inc

Advanced Sterilization Products: STERRAD 100NX Sterilizer, Product Code 10104 Used to ste...

Oil mist filter fails allowing oil mist to be emitted into the vicinity of the sterilizer, which may result in the release of a mist, "haze," or "smoke."

FDAFeb 25, 2008PR• Advanced Sterilization Products

Advanced Sterilization Products: STERRAD 50 Sterilization System, Product Code 10050 Used...

Oil mist filter fails allowing oil mist to be emitted into the vicinity of the sterilizer, which may result in the release of a mist, "haze," or "smoke."

FDAFeb 25, 2008PR• Advanced Sterilization Products

Advanced Sterilization Products: STERRAD NX Sterilizer, Product Code 10033 Used to steril...

Oil mist filter fails allowing oil mist to be emitted into the vicinity of the sterilizer, which may result in the release of a mist, "haze," or "smoke."

FDAFeb 25, 2008PR• Advanced Sterilization Products

Advanced Sterilization Products: STERRAD 100S Sterilization System, Product Code 10101 Us...

Oil mist filter fails allowing oil mist to be emitted into the vicinity of the sterilizer, which may result in the release of a mist, "haze," or "smoke."

FDAFeb 25, 2008PR• Advanced Sterilization Products