Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Atrium Medical Corporation

Atrium Medical Corporation Recalls

All product recalls associated with Atrium Medical Corporation.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 22741–22760 of 25000 recalls

Atrium Medical Corporation: HydraGlide Heparin coated PVC Straight Thoracic Catheters...

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

FDAMay 12, 2008Nationwide• Atrium Medical Corporation

Hitachi Medical Systems America Inc: EUB-9500/HI VISION 8500 Diagnostic Ultrasound Scanners, ...

The firm's parent company discovered a DICOM UID (Universal Identifier) code mix-up which can occur due to a software error. This error can cause the images from two (2) different patient scans to become intermingled and consequently, labeled incorrectly.

FDAMay 12, 2008AR, CA, IN +1 more• Hitachi Medical Systems America Inc

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

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

1...1136 113711381139 1140...1250

Page 1138 of 1250Next

FDA

May 12, 2008

Nationwide

• Atrium Medical Corporation

Hitachi Medical Systems America Inc: EUB-6500/HI VISION 6500 Diagnostic Ultrasound Scanners, D...

FDAMay 12, 2008AR, CA, IN +1 more• Hitachi Medical Systems America Inc

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

Opti Medical Systems Inc: Vitrex Blood Gas Capillary Tubes, MC0024, REF 189301, 250...

This lot of Heparinized Capillary Tubes contain contaminated lithium heparin.

FDAMay 8, 2008PR• Opti Medical Systems Inc

Hamilton Co: Hamilton Soft Grip Pipettes, 1 ml fixed volume, model num...

Manufacturing issue with spring may restrict product to drawing less than 1/2 of its stated measured capacity

FDAMay 7, 2008PR• Hamilton Co

Playground Swing Sets (Playworld) – Fall Hazard (2008)

Swing sets involved in this recall have the following part numbers: 8 ft 2-Unit Standard Swing 0248 5 in Arch Swing w-8 ft Top Rail 0287 8 ft Standard Duty Swing Add-A-Bay 0230 5 in Arch Swing 2-Unit Add-A-Bay 0370 10 ft 2-Unit Standard Swing 0249 3-1/2 in Arch Swing w-8 ft Top Rail 0288 10 ft Standard Duty Swing Add-A-Bay 0231 3-1/2 in Arch Swing Add-A-Bay 0375 8 ft 2-Unit Heavy Duty Swing 0270 2-3/8 in Arch Swing w-7 ft Top Rail 0120 8 ft heavy duty swing add-a-bay 0232 2-3/8 in Arch Swing Add-A-Bay 0121 10 ft 2-Unit Heavy Duty Swing 0259 7 ft Early Childhood T-Swing 0290 10 ft Heavy Duty Swing Add-A- Bay 0233 8 ft Single Post Swing Assembly 0295 8 ft Single Post Swing Add-A- Bay 0296

CPSCMay 6, 2008Nationwide• Playworld Systems Inc., of Lewisburg, Pa.

Weil-McLain CGs Gas Boilers – Carbon Monoxide Risk (2008)

Fire/Burn Risk

The recall involves cast iron, gas-fired boilers used for space heating. The following model names and serial numbers are included in the recall: Model Name Serial Numbers CGs-3, CGs-4, CGs-5, CGs-6 From CP 5071501 through CP 5694976 CGi-3, CGi-5, CGi-6 Series 2 From CP 4134351 through CP 5698635 The model name and serial number are located on separate labels on the outside of the left panel.

CPSCMay 6, 2008Nationwide• Weil-McLain, of Michigan City, Ind.

Williamson-Thermoflo Gas Boilers – Carbon Monoxide Risk (2008)

Fire/Burn Risk

The recall involves cast iron, gas-fired boilers used for space heating. The following model names and serial numbers are included in the recall: Model Name Serial Numbers GWS-127, GWS-158 From CP 5160092 through CP 5663040 GWI-063, GWI-095, GWI-127, GWI-158 From CP 4363986 through CP 5699844 The model name and serial number are located on separate labels on the outside of the left panel.

CPSCMay 6, 2008Nationwide• Weil-McLain, of Michigan City, Ind.

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

Broil King Gas Grills (Onward) – Fire Risk (2008)

Fire/Burn Risk

This recall includes the Signet, Sovereign and Sovereign XL series gas grills. Signet series (model #'s starting with 986xxx) 400 sq. inch cooking surface with 3 burners and drop-down shelves; includes models with side and rear burners Sovereign series (model #'s starting with 987xxx) 450 sq. inch cooking surface with 3 burners and drop-down shelves; includes models with side and rear burners. Sovereign XL series (model #'s starting with 988xxx) 600 sq. inch cooking surface with 4 burners and drop-down shelves. The model number can be located on the back panel of the grill.

CPSCMay 5, 2008Nationwide• Onward Manufacturing Co., of Ontario, Canada

Gambro Renal Products, Inc.: Gambro Cartridge Blood Set, 0141080XXXC, is intended for ...

Dialysis tubing sets may have occlusions restricting blood flow.

FDAMay 2, 2008Nationwide• Gambro Renal Products, Inc.

Gambro Renal Products, Inc.: Gambro Cartridge Blood Set, 003410-510, is intended for s...

Dialysis tubing sets may have occlusions restricting blood flow.

FDAMay 2, 2008Nationwide• Gambro Renal Products, Inc.

Dako North America Inc.: PT Link Waterbath, Model#PT100. Lab Vision PT Module P...

Dako is recalling the PT Link Waterbath because of a possible electrical hazard. Specifically, if the heater pad under the reagent tank becomes wet, it may present an electrical shock hazard when the lid is open.

Class IIModerate

FDAMay 1, 2008Nationwide• Dako North America Inc.

Dako North America Inc.: PT Link Waterbath, Model#PT100. Lab Vision PT Module Plu...

FDAMay 1, 2008Nationwide• Dako North America Inc.

Philips Medical Systems (Cleveland) Inc: GEMINI PET/CT System, a diagnostic imaging system for fix...

The reason for this inspection is to determine if the Spindle Block Servo Controllers on the CT subsystem of potentially affected GEMINI PET/CT systems are susceptible to premature failure.

FDAMay 1, 2008AL, AZ, CA +32 more• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: GEMINI PET/CT System, a diagnostic imaging system for fix...

The reason for this inspection is to determine if the Spindle Block Servo Controllers on the CT subsystem of potentially affected GEMINI PET/CT systems are susceptible to premature failure.

Class IIModerate

FDAMay 1, 2008AL, AZ, CA +32 more• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems: Laerdal "HeartStart Defibrillator", model M5067A, under L...

Buttons Sticking - The On/Off and Shock buttons on the front panel of the device may stick in place when pressed and fail to respond to the button press, causing a delay in the delivery of a defibrillation shock when the system advises a shock.

FDAApr 30, 2008Nationwide• Philips Medical Systems

Philips Medical Systems: Phillips Medical Systems, SureSigns VS3 Vital Signs Monit...

Some users of SureSigns VS3 Signs Monitor may have assumed that the SpO2 Non-Pulsatile and SpO2 No Sensor technical alarms were enabled when the SureSigns VS3 Vital Signs Monitor was not in Interval non-invasive blood pressure (NBP) mode. These alarms are only enabled when interval NBP mode is selected. If when monitoring SpO2, the clinician does not notice when the sensor is no longer attached, the patient is not being monitored through Spo2.This could result in delay or lack of needed therapy. The labeling provided with the monitor did not fully describe this feature.

FDAApr 30, 2008Nationwide• Philips Medical Systems