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Health product recall

Weck Electrosurgical Coagulation Suction Tube (2013-12-18)

Starting date:
December 18, 2013
Posting date:
January 24, 2014
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-37655

Recalled Products

  1. Weck Electrosurgical Coagulation Suction Tube 

Reason

The sterility of the product cannot be guaranteed.

Affected products

A. Weck Electrosurgical Coagulation Suction Tube 

Lot or serial number
  • 01A1100610
Model or catalog number
  • 809610
Companies
Manufacturer

Teleflex Medical

2917 Wreck Drive,

Research Triangle Park

27709

North Carolina

UNITED STATES