ASI 2.0 Instruments Calcar Trimmer Shaft (2019-08-14)

Starting date:

August 14, 2019

Posting date:

August 30, 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-70841

Last updated: 2019-09-05

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  Reason
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  Affected products

Produits touchés

ASI 2.0 Instruments Calcar Trimmer Shaft

Reason

Zimmer Biomet is conducting a lot specific medical device recall for the Calcar Trimmer Shaft. The potential issue associated with the instrument is that the end of the shaft could fail to effectively mate with the broach.

Affected products