Teleflex Disposable Aortic Punch (2020-01-14)

Starting date:

January 14, 2020

Posting date:

January 31, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-72223

Last updated: 2020-01-31

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  Reason
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  Affected products

Affected Products

Teleflex Disposable Aortic Punch

Reason

Teleflex is recalling the above product as there is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.

Affected products