Health product recall

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

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

Intramedullary Bone Saw Cam Assembly

Lot or serial number

25800
25810
81640
334360
366670
366680

Model or catalog number

475660
475665

Companies
Manufacturer
Biomet Orthopedics
56 East Bell Drive, P.O. BOX 587
Warsaw
46581
Indiana
UNITED STATES