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Implants & Prosthetics
Implants & Prosthetics
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Implants & Prosthetics
(225)
Monitoring Devices
(272)
Diagnostic Equipment
(819)
Home Healthcare
(232)
Contact Lenses & Vision
(17)
Surgical Equipment
(890)
225 recalls
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Centinel Spine
Medium Risk
FDA Device
Centinel Spine Prodisc C SK Cervical Discs Recalled for Labeling Mix-Up
Sold in 8 states
Sold at Authorized medical distributors, Direct to hospitals
Recalled
May 1, 2026
Added
May 2, 2026
DEPUY (IRELAND)
Medium Risk
FDA Device
Depuy Synthes Attune Revision Hinge Femoral Implants Recalled
Sold in Minnesota, North Carolina, Texas
Sold at Hospital and clinical supply chains
Recalled
Apr 29, 2026
Added
Apr 30, 2026
Straumann USA
Medium Risk
FDA Device
Straumann n!ce Dental Implant Restorations Recalled for Incorrect Screw Seat
Sold in 8 states
Sold at Dental clinics, Oral surgery centers +1 more
Recalled
Apr 29, 2026
Added
Apr 30, 2026
Boston Scientific
Critical Risk
FDA Device
Boston Scientific Pacemakers and CRT-Ps Recalled for Software Update
Distributed nationwide
Sold at Hospitals, Medical Facilities +1 more
1,404,232 units affected
Recalled
Apr 24, 2026
Added
Apr 25, 2026
Abbott Vascular
Critical Risk
FDA Device
Abbott Vascular: Absorb Bioresorbable Vascular Scaffold System Recalled for Heart Event Risks
Elevated rates of myocardial infarction and scaffold thrombosis compared to metallic stents
Recalled
Jun 1, 2017
Added
Apr 9, 2026
Encore Medical
Medium Risk
FDA Device
Encore Medical, LP: Shoulder and Knee Implants Recalled for Mislabeling
Sold in 11 states
Sold at Hospitals, Surgical Centers
Recalled
Jan 2, 2024
Added
Apr 7, 2026
SynCardia Systems
Medium Risk
FDA Device
SynCardia Systems LLC: SynCardia 50cc TAH-t Artificial Heart Recalled for Unreviewed Epoxy Resin
Sold in 15 states
Sold at Specialized Medical Centers, Hospitals
Recalled
Oct 20, 2023
Added
Apr 7, 2026
Medtronic Neuromodulation
Medium Risk
FDA Device
Medtronic Neuromodulation: DBS Lead with StimLoc Kit Recalled for Use By Date Label Discrepancy
Sold in 4 states
Sold at Authorized medical distributors
Recalled
Nov 3, 2023
Added
Apr 7, 2026
Townsend Design
Medium Risk
FDA Device
Townsend Design: Custom Sprystep and Vector Orthoses Recalled for Structural Breakage Risk
Sold in 48 states
Sold at Orthotics clinics, Healthcare providers +1 more
Recalled
Jan 5, 2024
Added
Apr 7, 2026
Genentech
Low Risk
FDA Drug
Genentech Susvimo (Ranibizumab Injection) Recalled for Defective Implants
Distributed nationwide
Sold at hospitals, specialty pharmacies +1 more
A few patients have experienced an issue with the implants that renders it non-functioning.
Recalled
Nov 1, 2022
Added
Apr 7, 2026
Straumann USA
Medium Risk
FDA Device
Straumann Custom Abutments Recalled for Material Manufacturing Mix-up
Sold in 10 states
Sold at Nationwide dental practitioners, Specialty dental clinics
Recalled
Mar 24, 2026
Added
Apr 6, 2026
Mentor Texas
Medium Risk
FDA Device
Mentor Breast Tissue Expanders Recalled for Dull or Breaking Needles
Distributed nationwide
Sold at Hospital supply chains, Medical device distributors +1 more
Recalled
Mar 27, 2026
Added
Apr 6, 2026
Tornier
Medium Risk
FDA Device
Tornier HRS Max Shoulder Replacement Parts Recalled for Mislabeling
Sold in 32 states
Sold at Tornier, Inc., Medical device distributors
Recalled
Apr 3, 2026
Added
Apr 6, 2026
Medium Risk
FDA Device
Endo-Model SL Connection Components and Replacement Plateaus Recalled
Sold in New Jersey
Sold at surgical centers, hospitals +1 more
Recalled
Mar 10, 2026
Added
Mar 23, 2026
MICROVENTION
Medium Risk
FDA Device
FRED 27 and FRED X 27 Flow Diverters Recalled for Improper Device Opening
Sold in 8 states
Sold at Clinical medical centers, Authorized neurovascular distributors
Recalled
Oct 10, 2025
Added
Mar 22, 2026
Prismatik Dentalcraft
Medium Risk
FDA Device
Glidewell HT Implant Twist Drills Recalled for Packaging Mix-Up
Sold in 6 states
Sold at Direct distribution
Recalled
May 28, 2025
Added
Mar 21, 2026
Medium Risk
FDA Device
Waldemar Link GmbH & Co. KG (Mfg Site): BiMobile Dual Mobility System Liner Recalled Due to Mislabeled Packaging
Sold in 4 states
Sold at Authorized medical distributors
Recalled
Feb 29, 2024
Added
Mar 21, 2026
LeMaitre Vascular
Medium Risk
FDA Device
Artegraft Collagen Vascular Grafts Recalled for Documentation Errors
Sold at Medical Distributors, Hospitals
Recalled
Oct 8, 2025
Added
Mar 21, 2026
Straumann USA
Medium Risk
FDA Device
Straumann WB XL Anatomic Healing Abutment XC Recalled for Incorrect Labeling
Distributed nationwide
Sold at Authorized dental supply distributors, Dental clinics +1 more
Recalled
Apr 24, 2025
Added
Mar 21, 2026
Medtronic Neuromodulation
Medium Risk
FDA Device
Medtronic Neuromodulation: Intellis Clinician Programmer Application Recalled for Connection Issues
Sold at Specialized medical distributors
Recalled
Jan 22, 2024
Added
Mar 21, 2026
MicroPort Orthopedics
Medium Risk
FDA Device
MicroPort Orthopedics Inc.: Evolution MP Femoral Knee Implants Recalled for Packaging Error
Sold at International distribution, China
One confirmed incident where the wrong part was found inside the packaging during surgery.
Recalled
Jul 1, 2024
Added
Mar 21, 2026
Abbott Medical
Medium Risk
FDA Device
Abbott Medical: Aveir Leadless Pacemaker Recalled Due to Potential Mode Change Interference
Sold in 50 states
Sold at Hospitals, Medical Centers +1 more
10,610 units affected
Recalled
Apr 29, 2024
Added
Mar 21, 2026
Medtronic Neuromodulation
Medium Risk
FDA Device
Medtronic Neuromodulation: Neurostimulators Recalled for MRI Compatibility Limitations
Distributed nationwide
Sold at hospitals, surgical centers +1 more
18,010 units affected
Recalled
Jul 24, 2024
Added
Mar 21, 2026
Medtronic Neuromodulation
Medium Risk
FDA Device
Medtronic Neuromodulation: Model 97745 Neurostimulator Controllers Recalled for Incorrect Language Firmware
Distributed nationwide
Sold at International distributors in South Korea and Turkey
Recalled
Nov 20, 2023
Added
Mar 21, 2026
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