This page has been archived on the Web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

WECK AUTO ENDO5 AUTOMATIC HEM-O-LOK CLIP APPLIERS (2017-10-02)

Starting date:
October 2, 2017
Posting date:
November 10, 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-65054

Affected products

WECK AUTO ENDO5 AUTOMATIC HEM-O-LOK CLIP APPLIERS

Reason

The devices being recalled are surgical clip appliers that are preloaded for use in minimally invasive surgical procedures. Teleflex is recalling these devices because they have a nonconformity that may cause clips to misload, jam or fall out of the appliers.

Affected products

WECK AUTO ENDO5 AUTOMATIC HEM-O-LOK CLIP APPLIERS

Lot or serial number

73B1700567

73F1600039

73H1600583

73K1600118

73K1600457

73M1600201

73M1600202

Model or catalog number

AE05ML

Companies
Manufacturer

Teleflex Medical

2917 Weck Drive

Research Triangle Park

27709

North Carolina

UNITED STATES