International Medical Devices Database

Source
RLMPH
1 Event
- Recall of AccuLIF PL Cages

One device in the database

AccuLIF PL Cages

Model / Serial

29 manufacturers with a similar name

Learn more about the data here

Howmedica Osteonics Corp. || Stryker Corporation

Manufacturer Parent Company (2017)
Stryker
Source
NIDFSINVIMA

HOWMEDICA OSTEONICS CORP (STRYKER ORTHOPAEDICS)

Manufacturer Parent Company (2017)
Stryker
Source
MSHM

STRYKER ORTHOPAEDICS MAHWAH - HOWMEDICA OSTEONICS CORP

Manufacturer Parent Company (2017)
Stryker
Source
MSHM

Stryker Howmedica Osteonics Corp.

Manufacturer Address
Stryker Howmedica Osteonics Corp., 325 Corporate Dr, Mahwah NJ 07430-2002
Manufacturer Parent Company (2017)
Stryker
Source
USFDA

Stryker Howmedica Osteonics Corp.

Manufacturer Address
Stryker Howmedica Osteonics Corp., 325 Corporate Dr, Mahwah NJ 07430-2006
Manufacturer Parent Company (2017)
Stryker
Source
USFDA

24 more

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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