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Health product recall

Biomet Suture Anchors and Retrievers (2016-04-06)

Starting date:
April 6, 2016
Posting date:
April 29, 2016
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-58120

Affected Products

A. ARTIFICIAL LIGAMENT FIXATION DEVICE ZIPLOOP EXT. TOGGLELOC TI ALLOY POLY. JUGGERKNOT SINGLE LOADED

B. JUGGERKNOT SINGLE LOADED

C. 2.9MM JUGGERKNOT

D. EZ PASS

Reason

Zimmer Biomet has initiated this action following an investigation which identified that specific lots produced may have an inadequate adhesive transfer from the Tyvek to the film. A weak seal may be evident.

Affected products

A. ARTIFICIAL LIGAMENT FIXATION DEVICE ZIPLOOP EXT. TOGGLELOC TI ALLOY POLY. JUGGERKNOT SINGLE LOADED

Lot or serial number

652430

652440

Model or catalog number

904755

Companies
Manufacturer

Biomet Sports Medicine

56 EAST BELL DRIVE P.O. BOX 587

WARSAW

Indiana

UNITED STATES



B. JUGGERKNOT SINGLE LOADED

Lot or serial number

649010

649050

Model or catalog number

912030

Companies
Manufacturer

Biomet Sports Medicine

56 EAST BELL DRIVE P.O. BOX 587

WARSAW

Indiana

UNITED STATES



C. 2.9MM JUGGERKNOT

Lot or serial number

654850

Model or catalog number

912029

Companies
Manufacturer

Biomet Sports Medicine

56 EAST BELL DRIVE P.O. BOX 587

WARSAW

Indiana

UNITED STATES



D. EZ PASS

Lot or serial number

673790

Model or catalog number

904051

Companies
Manufacturer

Biomet Sports Medicine

56 EAST BELL DRIVE P.O. BOX 587

WARSAW

Indiana

UNITED STATES