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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 581–600 of 4099 recalls

Ocean Water Seal Chest Drains (Atrium) – Setup Instructions (2023)

Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest drains do not provide sufficient precaution instruction for proper set up of catheter(s) and patient tube connections with single collection chamber chest drains

FDASep 18, 2023Nationwide• Atrium Medical Corporation

Express Dry Seal Chest Drains (Atrium) – Setup Instructions (2023)

FDASep 18, 2023Nationwide• Atrium Medical Corporation

Oasis Dry Suction Chest Drains (Atrium) – Setup Instructions (2023)

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FDASep 18, 2023Nationwide• Atrium Medical Corporation

EVIS EXERA III Video System (Olympus) – Power Supply Issue (2023)

Certain serial numbers of the CV-190 do not start up properly because parts that deviated from the specification were assembled into the power supply unit.

FDASep 14, 2023Nationwide• Olympus Corporation of the Americas

RayCare (RaySearch) – Document Visibility Issue (2023)

An issue was found in RayCare 5B, 6A, including service packs, where values will not be visible for documents in a read-only state when opened outside the Documents workspace when using document fields configured with single- or multi-selectable values.

FDASep 12, 2023MD, TN• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Thunderbeat Surgical Device (Olympus) – Button Malfunction (2023)

Thunderbeats blue seal button may remain in the engaged position after the button is released and not immediately return to a neutral position may result in prolonged surgery

FDASep 12, 2023Nationwide• Olympus Corporation of the Americas

Thunderbeat Surgical Device (Olympus) – Button Malfunction (2023)

Thunderbeats blue seal button may remain in the engaged position after the button is released and not immediately return to a neutral position may result in prolonged surgery

FDASep 12, 2023Nationwide• Olympus Corporation of the Americas

F2-01 Patient Monitor (GE Medical) – Data Communication Interruption (2023)

There is a potential interruption of data communication between E-modules inserted in the F2-01 Frame and CARESCAPE ONE and CARESCAPE Canvas 1000 patient monitors if the F2-01 Frame has not been powered down within the last 120 days.

FDASep 8, 2023Nationwide• GE Medical Systems China Co., Ltd. National Hi-Tech No.

Commercial Clothes Dryers (Whirlpool) – Fire hazard (2023)

Fire/Burn Risk

This recall involves all ADC brand stacked commercial clothes dryers with a 30 lb. capacity and model number ADG-30X2R or ADG-30X2Ri. Both models were sold in on-premise and coin-operated configurations for multi-unit housing, laundromats, and other facilities that use commercial laundry equipment. Logos and branding may appear differently depending on when the unit was manufactured. The model number for each unit is printed inside near the hinges of the upper door. The ADG-30X2R units were also sold in custom colors other than white to fit location branding.

CPSCSep 7, 2023Nationwide• Whirlpool Corporation, of Benton Harbor, Michigan

LP Gas Compact Regulators (Engineered Controls) – Fire hazard (2023)

Fire/Burn Risk

This recall involves the RegO 302 Series Compact Regulators with dates codes between 09/22 and 02/23. Regulators with the date code 21/22 are also included in this recall. The date codes are stamped on the back of the metal regulators. The regulators are designed for liquefied petroleum gas (i.e., propane) tanks for outdoor grills, heaters and fireplaces.

CPSCSep 7, 2023Nationwide• Engineered Controls International LLC, of Elon, North Carolina

RX Monaco Analyzer (Randox) – Rerun Setting Failure (2023)

RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for Auto reruns, not meeting sample re-run conditions when samples are above or below assay range and may result i issues with the re-run feature conditions when incorrectly. Potential to report incorrectly.

FDASep 6, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

RX Daytona Analyzer (Randox) – Rerun Setting Failure (2023)

FDASep 6, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

RX Imola Analyzer (Randox) – Rerun Setting Failure (2023)

FDASep 6, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Venue Go Standard Cart (GE Medical) – Tilt Mechanism Failure (2023)

Some Venue Go Standard Carts can develop an internal failure of the vertical/horizontal tilt adjustment mechanism which can result in the Venue Go system detaching from the cart and falling.

FDASep 6, 2023Nationwide• GE MEDICAL SYSTEMS, ISRAEL LTD. Nativ Haa??or Street no.

RX Daytona Plus Clinical Chemistry Analyzer (Randox) – rerun settings issue (2023)

FDASep 6, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

RX Modena Clinical Chemistry Analyzer (Randox) – rerun settings issue (2023)

FDASep 6, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Oasis Dry Suction Water Seal Chest Drain (Atrium) – unauthorized reprocessing (2023)

Product was re-processed and re-sterilized by a third party using packaging configurations and a sterilization process which are not approved by the manufacture and lack validation.

FDASep 5, 2023VA• Atrium Medical Corporation

Life Is Peachy Ice Cream (Life Raft) – Listeria contamination (2023)

Listeria

South Carolina Department of Health discovered the product contained Listeria monocytogenes.

Class IHigh

FDASep 5, 2023DC• Life Raft Treats Ice Cream Factory

Ice Cream Not Fried Chicken (Life Raft) – Listeria contamination (2023)

Listeria

South Carolina Department of Health discovered the product contained Listeria monocytogenes.

Class IHigh

FDASep 5, 2023DC• Life Raft Treats Ice Cream Factory

Ski-Doo and Lynx Snowmobiles (BRP) – Fire Hazard (2023)

Fire/Burn Risk

This recall involves all model year 2023 Ski-Doo Freeride and Summit model snowmobiles equipped with an 850E-TEC Turbo R Engine and all Lynx Shredder model snowmobiles equipped with an 850 E-TEC Turbo R Engine. The vehicles were sold in a variety of colors. "Ski-Doo" is printed on a decal on the right-hand side of the snowmobiles. A vehicle decal is printed on the side of the snowmobiles that includes the model name. Only snowmobiles with the following years and model numbers are included in the recall: Model Year Model Name 2023 Ski-Doo Freeride 850 E-TEC Turbo R 2022 Ski-Doo Summit 850 E-TEC Turbo R 2023 Lynx Shredder 850 E-TEC Turbo R

CPSCAug 31, 2023Nationwide• Bombardier Recreational Products Inc., of Canada