Health product recall

JOURNEY Knee System - Femoral OXINIUM and COCR Nonporous Bi-Cruciate Stabilized (BCS) (2018-06-19)

Starting date:
June 19, 2018
Posting date:
July 5, 2018
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-67186

Affected products

A. JOURNEY Knee System - Femoral OXINIUM Nonporous Bi-Cruciate Stabilized (BCS)

B. JOURNEY Knee System - Femoral COCR Nonporous Bi-Cruciate Stabilized (BCS)

Reason

The analysis of available post-market surveillance data suggests that patients that have been implanted with a first generation JOURNEY BCS Knee System may have a higher risk of requiring a revision earlier than they or their surgeon had expected.

Affected products

A. JOURNEY Knee System - Femoral OXINIUM Nonporous Bi-Cruciate Stabilized (BCS)

Lot or serial number

All lots.

Model or catalog number

74021110

74021111

74021112

74021113

74021114

74021115

74021116

74021117

74021118

74021119

74021120

74021121

74021122

74021123

74021124

74021125

74021126

74021127

74021128

74021129

Companies
Manufacturer

Smith & Nephew Inc.

1450 Brooks Road

Memphis

38116

Tennessee

UNITED STATES


B. JOURNEY Knee System - Femoral COCR Nonporous Bi-Cruciate Stabilized (BCS)

Lot or serial number

All lots.

Model or catalog number

74021210

74021211

74021212

74021213

74021214

74021215

74021216

74021217

74021218

74021219

74021220

74021221

74021222

74021223

74021224

74021225

74021226

74021227

74021228

74021229

Companies
Manufacturer

Smith & Nephew Inc.

1450 Brooks Road

Memphis

38116

Tennessee

UNITED STATES