International Medical Devices Database

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
RLMPH
1 Event
- Recall of Sterilmed reprocessed agilis steerable introducer sheas

One device in the database

Sterilmed reprocessed agilis steerable introducer sheas

Model / Serial

4 manufacturers with a similar name

Learn more about the data here

STERILMED, INC.

Manufacturer Address
STERILMED, INC., 11400 73rd Ave N, Maple Grove MN 55369-5561
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

Sterilmed Inc

Manufacturer Address
Sterilmed Inc, 5010 Cheshire Pkwy N Ste 2, Minneapolis MN 55446-4101
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

Sterilmed Inc

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
DH

Sterilmed Inc

Manufacturer Address
Sterilmed Inc, 11400 73rd Ave N Ste 100, Osseo MN 55369-5562
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

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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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