Manufacturer

Atrium Medical Corporation

150 recalls in our database name Atrium Medical Corporation as the manufacturing or recalling firm.

What the numbers show

Total: 150
Critical: 2
Severe: 4
Most recent: 2024-10-16

Of the 150 recalls from Atrium Medical Corporation we have scored against our rubric, 2 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (3%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

126–150 of 150

HighFDA (Devices)·Z-0735-2014·2014-01-22
Atrium Ocean Water Seal Chest Drain ATS Blood Recovery System Recall
Atrium Medical Corporation is recalling Ocean Water Seal Chest Drain ATS Blood Recovery Systems because the tubing may leak or disconnect.
Product
Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery System with stopcock and in-line connectors; Product Code: 2050-000. To evacuate air and/or fluid from the chest cavity or mediastinum.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0738-2014·2014-01-22
Atrium Ocean Water Seal Chest Drain ATS Blood Recovery System Recalled
Atrium Medical Corporation is recalling 361 units of the Ocean Water Seal Chest Drain ATS Blood Recovery System because the tubing may leak or disconnect.
Product
Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery System Dual patient lines with stopcock and in-line connectors Product Code: 2052-000. To evacuate air and/or fluid from the chest cavity or mediastinum.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0739-2014·2014-01-22
Atrium Ocean Water Seal Chest Drain ATS Blood Recovery System Recall
Atrium Medical Corporation is recalling 1,002 units of Ocean Water Seal Chest Drain ATS Blood Recovery Systems due to potential tubing leaks or disconnections.
Product
Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery System Dual patient lines with stopcock; .Product Code: 2052-300. To evacuate air and/or fluid from the chest cavity or mediastinum.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0740-2014·2014-01-22
Atrium Oasis Chest Drain Tubing Recalled for Leak or Disconnect Risk
Atrium Medical Corporation is recalling Oasis Dry Suction Water Seal ATS Chest Drains because the tubing may leak or disconnect.
Product
Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery System Chest Drain with in-line connectors Product Code: 3650-100. To evacuate air and/or fluid from the chest cavity or mediastinum.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0741-2014·2014-01-22
Atrium Oasis Chest Drain Tubing Recalled for Leak or Disconnect Risk
Atrium Medical Corporation is recalling 954 units of Oasis Dry Suction Water Seal ATS Chest Drains because the tubing may leak or disconnect.
Product
Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery System Chest Drain Dual patient lines; Product Code: 3652-100. To evacuate air and/or fluid from the chest cavity or mediastinum.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0736-2014·2014-01-22
Atrium Ocean Water Seal Chest Drain tubing may leak or disconnect
Atrium Medical Corporation is recalling 624 units of Ocean Water Seal Chest Drain ATS Blood Recovery Systems because the tubing may leak or disconnect.
Product
Atrium Ocean Water Seal Chest Drain ATS Blood Recovery System with stopcock and in-line connectors Sterile fluid path packaging Product Code: 2050-070. To evacuate air and/or fluid from the chest cavity or mediastinum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2304-2013·2013-10-09
Atrium Medical Recalls Advanta VXT Vascular Grafts Due to Label Adhesion
Atrium Medical Corporation is recalling Advanta VXT Vascular Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Advanta VXT Vascular Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2309-2013·2013-10-09
Atrium Medical Recalls Advanta VS Grafts Due to Label Adhesion Issue
Atrium Medical Corporation is recalling Advanta VS Grafts because the inner tray label may adhere to the outer tray, making removal difficult.
Product
Advanta VS Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2306-2013·2013-10-09
Atrium Medical Recalls Advanta SuperSoft Grafts Due to Label Adhesion
Atrium Medical Corporation is recalling Advanta SuperSoft Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Advanta SuperSoft Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2308-2013·2013-10-09
Atrium Medical Recalls Advanta SST Bifurcated Grafts Due to Label Adhesion
Atrium Medical Corporation is recalling Advanta SST Bifurcated Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Advanta SST Bifurcated Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2313-2013·2013-10-09
Atrium Medical Recalls Advanta VXT Grafts Due to Label Adhesion Issue
Atrium Medical Corporation is recalling Advanta VXT Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Advanta VXT Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2312-2013·2013-10-09
Atrium Medical Recalls Advanta SuperSoft Grafts Due to Label Adhesion
Atrium Medical Corporation is recalling Advanta SuperSoft Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Advanta SuperSoft Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2310-2013·2013-10-09
Atrium Flixene Grafts Recalled Due to Difficult-to-Remove Inner Tray Label
Atrium Medical Corporation is recalling Flixene Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Flixene Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2307-2013·2013-10-09
Atrium Flixene IFG Recall Due to Label Adhesion Issue
Atrium Medical Corporation is recalling Flixene IFG with Assisted Delivery because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Flixene IFG with Assisted Delivery Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2314-2013·2013-10-09
Atrium Flixene Grafts Recalled Due to Difficult Tray Removal
Atrium Medical Corporation is recalling Flixene Trumpet Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Flixene Trumpet Grafts >or= 6mm Flixene GW and GWT Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2317-2013·2013-10-09
Atrium Medical Recalls Advanta SST Grafts Due to Label Adhesion
Atrium Medical Corporation is recalling Advanta SST Grafts because the inner tray label may adhere to the outer tray, making removal difficult.
Product
Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2311-2013·2013-10-09
Atrium Medical Recalls Advanta SST Grafts Due to Label Adhesion
Atrium Medical Corporation is recalling Advanta SST Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Advanta SST Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2315-2013·2013-10-09
Atrium Medical Recalls Advanta VS Grafts Due to Label Adhesion
Atrium Medical Corporation is recalling Advanta VS Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Advanta VS Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2305-2013·2013-10-09
Atrium Flixene IFG Vascular Grafts Recalled for Label Adhesion Issue
Atrium Medical Corporation is recalling Flixene IFG Vascular Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Flixene IFG Vascular Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2316-2013·2013-10-09
Atrium Medical Recalls Advanta SST Grafts Due to Label Adhesion Issue
Atrium Medical Corporation is recalling Advanta SST Grafts because the inner tray label may adhere to the outer tray, making it difficult to remove the tray onto the sterile field.
Product
Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1987-2013·2013-08-28
Atrium Medical Recalls PleuraGuide Chest Tube Kits Due to Missing Instructions
Atrium Medical Corporation is recalling 6,516 PleuraGuide Disposable Chest Tube Kits because individual component instructions for use are missing.
Product
PleuraGuide Disposable Chest Tube Kit; Product codes: 17100, 17150, and 17200. Indicated to assist with the insertion of thoracic catheters.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1939-2013·2013-08-21
Atrium Medical Recalls C-QUR TacShield Mesh Due to Packaging Adhesion
Atrium Medical Corporation is recalling C-QUR TacShield Mesh units because the coated mesh can adhere to the inner packaging liner when exposed to high humidity.
Product
C-QUR TacShield Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1937-2013·2013-08-21
Atrium Medical Recalls C-QUR Edge Mesh Due to Packaging Adhesion
Atrium Medical is recalling C-QUR Edge Mesh products because the coated mesh can adhere to the inner packaging liner when exposed to high humidity.
Product
C-QUR Edge Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1936-2013·2013-08-21
Atrium Medical Recalls C-QUR Mesh Due to Packaging Adhesion Issues
Atrium Medical Corporation is recalling C-QUR Mesh products because the coated mesh can adhere to the inner packaging liner when exposed to high humidity.
Product
C-QUR Mesh (All Sizes, shapes). Intended for use in soft tissue deficiencies.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1938-2013·2013-08-21
Atrium Medical Recalls C-QUR V-Patch Mesh Due to Adhesion Issues
Atrium Medical Corporation is recalling C-QUR V-Patch Mesh units because the coated mesh may adhere to the inner packaging liner when exposed to high humidity.
Product
C-QUR V-Patch Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.
Category
Medical Device
Distribution
Distributed nationwide

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

ATRIUM MEDICAL CORPORATION

Source: Wikidata (Q139903018), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.