International Medical Devices Database

Manufacturer Parent Company (2017)
Abbvie Inc.
Source
AEMPSVFOI
1 Event
- Recall Or Safety Alert for AbbVie PEG 20FR probes, reference 62945-001, labeled as PEG Kit 20FR, lots 32085235, 32224175, 32282264

One device in the database

AbbVie PEG 20FR probes, reference 62945-001, labeled as PEG Kit 20FR, lots 32085235, 32224175, 32...

Model / Serial

7 manufacturers with a similar name

Learn more about the data here

AbbVie Inc.

Manufacturer Address
AbbVie Inc., 1 N Waukegan Rd, North Chicago IL 60064-1802
Manufacturer Parent Company (2017)
Abbvie Inc.
Source
USFDA

AbbVie Inc.

Manufacturer Parent Company (2017)
Abbvie Inc.
Source
BAM

AbbVie Inc.

Manufacturer Parent Company (2017)
Abbvie Inc.
Source
MHSIDCCCDMIS

AbbVie Inc.

Manufacturer Parent Company (2017)
Abbvie Inc.
Source
SMPA

AbbVie Inc.

Manufacturer Parent Company (2017)
Abbvie Inc.
Source
SATP

About this database

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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