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Health product recall

Cascade Pro-ES-IX Stimulator (2013-05-31)

Starting date:
May 31, 2013
Posting date:
September 26, 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-41539

Recalled products

  1.  Cascade Pro-ES-IX Stimulator

Reason

Ceramic core of the transformer may be susceptible to cracking, which causes the device to run at a higher temperature. Operating at a higher temperature may trigger the overheat protection circuitry and switches the unit off.

Affected products

A. Cascade Pro-ES-IX Stimulator

Lot or serial number
  • 1012CX25-00-007
  • 1012CX25-00-008
  • 1101CX25-00-024
  • 1102CX25-00-003
  • 1104CX25-00-024
  • 1104CX25-00-027
  • 1106CX25-00-027
  • 1112CX25-00-016
  • 1201CX25-00-012
  • 1207CX25-01-007
  • 1209CX25-01-028
Model or catalog number
  • 190262-200
Companies
Manufacturer
Cadwell,
909 North Kellogg Street,
Kennewick,
99336
Washington
UNITED STATES