This page has been archived on the Web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

Slideprep Plus Cytology Centrifuge (2013-06-19)

Starting date:
June 19, 2013
Posting date:
September 27, 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-35923

Recalled products

A. Slideprep Plus Cytology Centrifuge 

Reason

Slideprep Plus Cytology centrifuges manufactured prior to January 1, 2013 have the potential of starting up unexpectedly when encountering an electrostatic discharge, causing the rotor to possibly begin to spin.

Affected products

Slideprep Plus Cytology Centrifuge

Lot or serial number

More than 10 serial numbers, contact manufacturer 

Model or catalog number
  • 100-400
  • 100-401
  • 100-500
Companies
Manufacturer

Separation Technology Inc.

582 Monroe Road, Suite 1424,

Sanford

32771

Florida

UNITED STATES