International Medical Devices Database

Manufacturer Parent Company (2017)
A&E Medical Corporation
Source
NZMMDSA
1 Event
- Recall of A&E Aorta Punch

One device in the database

A&E Aorta Punch

Model / Serial
Model: , Affected: lot numbers from 0090P through 0230P

One manufacturer with a similar name

Learn more about the data here

A & E MEDICAL CORPORATION

Manufacturer Address
FARMINGDALE
Manufacturer Parent Company (2017)
A&E Medical Corporation
Source
HC

About this database

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

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

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.

Download the data

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.

Download all (zipped)

A & E Medical Corporation

One device in the database

A&E Aorta Punch

One manufacturer with a similar name

A & E MEDICAL CORPORATION