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Health product recall

Navigation II Cart - Articulating Arm (2015-05-19)

Starting date:
May 19, 2015
Posting date:
June 15, 2015
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-53797

Recalled Products

  1. Navigation II Cart - Articulating Arm

Reason

Stryker was notified by the supplier of the articulated arm that there was the potential for the weld seam between the main stud and the two flaps on the articulated arm to fail. The main welding process to manufacture the joint was not executed correctly and the weld may not be in the correct location.

Affected products

A. Navigation II Cart  - Articulating Arm

Lot or serial number
  • 100957
  • 100983
Model or catalog number
  • 7700-100-000
Companies
Manufacturer

Stryker Leibinger GmbH and Co. KG

Botzinger Strasse 41

Freiburg

79111

GERMANY