This page has been archived on the Web

Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.

Health product recall

Surgical and Laser Larygoscope (2013-11-18)

Starting date:
November 18, 2013
Posting date:
December 17, 2013
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-37219

Recalled products

  1. Surgical Laryngoscope, Spreadable
  2. Laser Laryngoscope

Reason

Laryngoscopes are class II devices in Canada and therefore have to be reclassified.

Affected products

A. Surgical Laryngoscope, Spreadable
 

Lot or serial number

Not applicable

Model or catalog number
  • 50-202-04
Companies
Manufacturer
Spiggle and Theis Medizintechnik GmbH
Burghof 14
Overath
51491
GERMANY

B. Laser Laryngoscope

Lot or serial number

Not applicable

Model or catalog number
  • 50-215-06
Companies
Manufacturer
Spiggle and Theis Medizintechnik GmbH
Burghof 14
Overath
51491
GERMANY