International Medical Devices Database

Source
SATP
1 Event
- Field Safety Notices about MYO/Punch, A&E Surgical Punch

One device in the database

MYO/Punch, A&E Surgical Punch

Model / Serial
080-271, 080-351, 080-401, 080-403, 080-451, 080-481, 080-501 | Affects all sterile surgical punches with lot numbers from 0090P through 0230P
Product Description
MD: Aorta punch, single-use

5 manufacturers with a similar name

Learn more about the data here

A&E Medical Corporation

Manufacturer Parent Company (2017)
A&E Medical Corporation
Source
BAM

A&E Medical Corporation

Manufacturer Parent Company (2017)
A & E Medical Corporation
Source
MHSIDCCCDMIS

A&E Medical Corporation

Manufacturer Parent Company (2017)
A & E Medical Corporation
Source
SMPA

A&E Medical Corporation

Manufacturer Parent Company (2017)
A&E Medical Corporation
Source
MHRA

A&E Medical Corporation

Manufacturer Parent Company (2017)
A&E Medical Corporation
Source
VNSAWH

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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