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Health product recall

Autolith Lithotripter System-Probes

Starting date:
March 29, 2017
Posting date:
June 21, 2017
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Hospitals, Healthcare Professionals
Identification number:
RA-63680

Reason

Specific lot of probe being recalled because they were labelled with an incorrect model number (9-202-3751DS).

Affected products

Autolith Lithotripter System-Probes

Lot or serial number

LDS12516

Model or catalog number

9-195-371DS

Companies

Manufacturer
Northgate Technologies Inc.
1591 Scottsdale Court
Elgin
60123
Illinois
UNITED STATES