Intramedullary Bone Saw Cam Assembly (2019-10-30)

Starting date:

October 30, 2019

Posting date:

November 29, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-71718

Last updated: 2019-12-02

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  Reason
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  Affected products

Affected Products

Intramedullary Bone Saw Cam Assembly

Reason

Zimmer Biomet is conducting a medical device recall for intramedullary bone saw cam assembly due to a possible commingle of 13 mm and 14 mm intramedullary bone saw cam assemblies. A complaint was received in which it was reported that an intramedullary bone saw cam assembly was labeled and etched as a 14 mm but measured as a 13 mm cam.

Affected products