NeoBurr Carbide Bur (2020-08-12)

Starting date:

August 12, 2020

Posting date:

September 4, 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-73859

Last updated:
2020-09-04

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  Reason
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  Affected products

Affected Products

NeoBurr Carbide Bur

Reason

The NeoBurr Carbide Bur was shipped with the possibility of a compromised sterile barrier. On July 24, 2020 it was determined the defective device was released to the market. On August 12, 2020 it was determined that the defective device was shipped to a Canadian customer.

Affected products