YUKON ANTI TORQUE ALIGNMENT TUBE (2020-10-28)

Starting date:

October 28, 2020

Posting date:

December 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-74467

Last updated:
2020-12-03

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  Reason
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  Affected products

Affected Products

YUKON ANTI TORQUE ALIGNMENT TUBE

Reason

Stryker received complaints (July 23, 2020) of reports of shafts not passing through the inner cannula of alignment tubes from lot KTGG. These events were later determined to be associated with a manufacturing non-conformance specific to lot KTGG.

Affected products