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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device prosthesis, hip, hemi-, femoral, metal ball
Regulation Description Hip joint femoral (hemi-hip) metallic cemented or uncemented prosthesis.
Product CodeLZY
Regulation Number 888.3360
Device Class 2


Premarket Reviews
ManufacturerDecision
SMITH & NEPHEW, INC.
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2021 59 59
2022 65 65
2023 77 77
2024 74 74
2025 77 77
2026 23 23

Device Problems MDRs with this Device Problem Events in those MDRs
Adverse Event Without Identified Device or Use Problem 325 325
Device Dislodged or Dislocated 27 27
Naturally Worn 11 11
Fracture 4 4
Device Contaminated During Manufacture or Shipping 3 3
Break 2 2
Degraded 2 2
Off-Label Use 1 1
Material Twisted/Bent 1 1
Material Deformation 1 1
Detachment of Device or Device Component 1 1
Migration 1 1
Appropriate Term/Code Not Available 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
Unspecified Infection 167 167
Pain 95 95
Joint Dislocation 34 34
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 21 21
Joint Laxity 17 17
Insufficient Information 14 14
No Clinical Signs, Symptoms or Conditions 11 11
Hematoma 6 6
Discomfort 6 6
Foreign Body Reaction 5 5
Unspecified Tissue Injury 5 5
Arthritis 5 5
Fluid Discharge 4 4
Bone Fracture(s) 3 3
Hypersensitivity/Allergic reaction 2 2
Inflammation 2 2
Fall 2 2
Pocket Erosion 2 2
Arthralgia 1 1
Failure of Implant 1 1
Metal Related Pathology 1 1
Adhesion(s) 1 1
Muscle Weakness 1 1
Cardiac Arrest 1 1
Post Operative Wound Infection 1 1
Thrombosis/Thrombus 1 1
Heart Failure/Congestive Heart Failure 1 1
Hemorrhage/Bleeding 1 1

Recalls
Manufacturer Recall Class Date Posted
1 BioPro, Inc. II Oct-14-2025
2 DePuy Orthopaedics, Inc. II Jul-12-2022
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