OCEAN 2050-300Recalls & reported problems
Atrium Medical Corporation · DRAIN, TOTAL RECOVERY W/S · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00650862103069), received between Sep 13, 2016 and Sep 13, 2016 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
22 other recalls cover devices cleared under the same FDA submission (K043582); they may or may not involve this specific model.
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.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Pneumothorax1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 13, 2016Insufficient Device Problem Information
REPORT RECEIVED STATED THE PATIENT HAD A RECURRENT PNEUMOTHORAX WHEN THE DRAIN WAS REMOVED FROM THE WALL SUCTION.
Patient problems: Pneumothorax
MAUDE report 5948242 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K043582. One submission often covers many models, so check the product and lot details in each record.
- Z-0486-2024 · Sep 5, 2023 · Open, ClassifiedAtrium Oasis Dry Suction Water Seal Chest Drain, Part Number: 3650-100, DRAIN, OASIS BRU W/AC, 3650 ATS BLOOD RECOVERY
- Z-0235-2023 · Oct 18, 2022 · Open, ClassifiedAtrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000
- Z-1607-2022 · May 25, 2022 · Open, ClassifiedGETINGE USA SALES LLC OCEAN Chest Drain System Atrium 2100 mL Model Number: 2002-000
- Z-0307-2022 · Oct 22, 2021 · Open, ClassifiedThe Ocean Water Seal Chest Drain is a plastic, three bottle vacuum collection device. It consists of a collection chamber that holds shed mediastinal blood, a water seal chamber us
- Z-1206-2017 · Dec 23, 2016 · TerminatedMaquet Ocean Water Seal Chest Drain, Single Collection w/AC Reference: 2002-100 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-estab
- Z-1205-2017 · Dec 23, 2016 · TerminatedMaquet Ocean Water Seal Chest Drain, Single Collection WAC Reference: 2002-000 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establ
- Z-1210-2017 · Dec 23, 2016 · TerminatedMaquet Express Dry Seal Suction OCEAN DRAIN, SINGLE Reference: 2002-400 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lun
- Z-1209-2017 · Dec 23, 2016 · TerminatedMaquet Express Dry Seal Suction OCEAN DRAIN, SINGLE W/S Reference: 2002-300 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish
- Z-1936-2015 · May 7, 2015 · TerminatedOcean Water Seal Chest Drain, SINGLE W/AC P/N: 2002-100
- Z-1935-2015 · May 7, 2015 · TerminatedOcean Water Seal Chest Drain, Single Collection W/AC, P/N: 2002-000
- Z-1937-2015 · May 7, 2015 · TerminatedOasis Dry Suction Water Seal Chest Drain, DRY SINGLE W/AC P/N: 3600-100
- Z-1938-2015 · May 7, 2015 · TerminatedEXPRESS Dry Seal Chest Drain, Single Collection P/N: 4000-100N
- Z-1959-2014 · Apr 28, 2014 · TerminatedAtrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
- Z-0736-2014 · Nov 19, 2013 · TerminatedAtrium 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 f
- Z-0740-2014 · Nov 19, 2013 · TerminatedAtrium 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
…and 7 more.
Other Apparatus, Autotransfusion devices
- OASIS 3650-100Atrium Medical Corporation · APPARATUS, AUTOTRANSFUSION2 recalls22 reports
- EXPRESS 4050-100NAtrium Medical Corporation · APPARATUS, AUTOTRANSFUSION2 recalls2 reports
- NA ATL2001Medtronic, Inc. · APPARATUS, AUTOTRANSFUSION1 death79 reports
- autoLog IQ™ ATLGIQMedtronic, Inc. · APPARATUS, AUTOTRANSFUSION58 reports
- NA BTC93Medtronic, Inc. · APPARATUS, AUTOTRANSFUSION1 recall2 reports
- OCEAN 2050-000Atrium Medical Corporation · Apparatus, Autotransfusion1 recall2 reports
- NA BTC98Medtronic, Inc. · APPARATUS, AUTOTRANSFUSION1 recall0 reports
- HAEMONETICS CELL SAVER ELITE SYSTEM CSE-P-125Haemonetics Corporation · Apparatus, Autotransfusion47 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.