This page has been archived on the Web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

Hologic MyoSure Rod Lens Hysteroscope (2017-12-11)

Starting date:
December 11, 2017
Posting date:
December 21, 2017
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
Healthcare Professionals, General Public, Hospitals
Identification number:
RA-65466

Affected products

Hologic MyoSure Rod Lens Hysteroscope

Reason

Hologic became aware that some users were not consistently following the cleaning instructions contained within the MyoSure Rod Lens Hysteroscope instructions for use (IFU).

Affected products

Hologic MyoSure Rod Lens Hysteroscope

Lot or serial number

All lots

Model or catalog number

40-250

50-250XL

Companies
Manufacturer

Hologic Inc.

250 CAMPUS DRIVE

MARLBOROUGH

01752

Massachusetts

UNITED STATES