International Medical Devices Database

Manufacturer Parent Company (2017)
Baxter International
Source
RLMPH
2 Events
- Recall of Revaclear 400, Lot 4-9502-H-01
- Recall of Prismaflex control unit (SW 7.11) used together with the PrismaLung Kit

2 devices in the database

Revaclear 400, Lot 4-9502-H-01

Model / Serial

Prismaflex control unit (SW 7.11) used together with the PrismaLung Kit

Model / Serial

113 manufacturers with a similar name

Learn more about the data here

Gambro Lundia AB

Manufacturer Parent Company (2017)
Baxter International
Source
NIDFSINVIMA

Gambro Lundia Ab

Manufacturer Parent Company (2017)
Baxter International
Source
NIDFSINVIMA

Gambro Renal Products, Inc.

Manufacturer Parent Company (2017)
Baxter International
Source
NIDFSINVIMA

Nipro Corporation || Quintin Instrument Co || Baxter Healthcare Corporation Of Puerto Rico || Alt...

Source
NIDFSINVIMA

Gambro Dialysatoren GmbH & Co KG

Manufacturer Parent Company (2017)
Baxter International
Source
NZMMDSA

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Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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