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Surgical Equipment
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Implants & Prosthetics
(228)
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(259)
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(818)
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(219)
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(17)
Surgical Equipment
(898)
898 recalls
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Merit Medical Systems
Medium Risk
FDA Device
Merit Medical Monarch Inflation Devices Recalled for Sterile Barrier Defect
Sold in 46 states
Sold at Hospitals, Medical clinics +1 more
Environmental bacteria (due to sterile barrier breach) contamination
Recalled
Oct 11, 2024
Added
Mar 21, 2026
Angiodynamics
Medium Risk
FDA Device
Angiodynamics, Inc.: Mini Stick Max Guidewire Introducers Recalled Due to Potential Blockage
Distributed nationwide
Sold at Angiodynamics, Inc., Hospitals +1 more
19,423 units affected
Recalled
Mar 21, 2024
Added
Mar 21, 2026
Medium Risk
FDA Device
Medline Medical Convenience Kits Recalled for Syringe Leaks and Breakage
Distributed nationwide
Sold at Specialty Healthcare Providers, Medical Supply Distributors +2 more
19,552 units affected
Recalled
Mar 26, 2025
Added
Mar 21, 2026
Medline Industries
Medium Risk
FDA Device
Medline Medical Convenience Kits Recalled for Compromised Sterile Packaging
Distributed nationwide
Sold at Hospital supply distributors, Direct medical sales
54,301 units affected
Recalled
Feb 9, 2026
Added
Mar 21, 2026
Stryker
Medium Risk
FDA Device
Stryker Corporation: ACM Mixing System Components Recalled Due to Risk of Breakage During Surgery
Distributed nationwide
Sold at surgical centers, hospitals
Foreign device components falling into surgical site contamination
Recalled
Sep 19, 2023
Added
Mar 21, 2026
Cook Biotech
Medium Risk
FDA Device
Cook Biotech, Inc.: Biodesign Fistula Plugs and Grafts Recalled for Early Expiration
Distributed nationwide
Sold at Hospital supply chains, Medical device distributors
Recalled
Sep 25, 2024
Added
Mar 21, 2026
Steris
Medium Risk
FDA Device
AMSCO 7052HP and 7053HP Washer/Disinfectors Recalled for Electrical Arcing
Sold in 18 states
Sold at Steris Corporation, Direct medical supply channels
Recalled
Dec 11, 2025
Added
Mar 21, 2026
MAQUET
Medium Risk
FDA Device
Maquet Corin Operating Tables Recalled for Electronic Interference Risk
Sold in Kentucky, New York, Texas
Sold at Medical distributors, Healthcare facilities
Recalled
Aug 22, 2025
Added
Mar 21, 2026
Boston Scientific
Medium Risk
FDA Device
Boston Scientific Corporation: WallFlex and Agile Esophageal Stents Recalled for Catheter Tip Detachment
Distributed nationwide
Sold at Authorized Medical Distributors, Hospitals +1 more
Recalled
Sep 26, 2024
Added
Mar 21, 2026
Synthes (USA) Products
High Risk
FDA Device
Synthes (USA) Products LLC: Various Sterile Orthopedic Implants and Tools Recalled for Sterility Failure
Distributed nationwide
Sold at Hospitals, Surgical Centers +1 more
Recalled
Mar 1, 2024
Added
Mar 21, 2026
Steris
Medium Risk
FDA Device
Steris Corporation: Medical Endoscope Hookups Recalled for Incorrect Disinfection Instructions
Distributed nationwide
Sold at Steris Corporation, Medical distributors
Pathogenic microorganisms due to improper disinfection contamination
Recalled
Aug 8, 2024
Added
Mar 21, 2026
Stryker Orthopaedics
Medium Risk
FDA Device
Stryker Orthopaedics: Mako Robotic-Arm Surgical Software Recalled for Error-Related Treatment Delays
Distributed nationwide
Sold at Stryker Orthopaedics Direct Sales, Authorized Medical Device Distributors
Recalled
May 28, 2024
Added
Mar 21, 2026
Baxter Healthcare
Medium Risk
FDA Device
Baxter Healthcare Corporation: Various Surgical Products Recalled Due to Inaccurate Marketing Information
Distributed nationwide
Sold at Authorized Medical Distributors, Direct Hospital Sales
Recalled
Jan 5, 2024
Added
Mar 21, 2026
Medium Risk
FDA Device
CleverCut and Olympus Single Use Sphincterotomes Recalled for Deforming Risk
Sold in 45 states
Sold at Authorized Medical Distributors, Specialty Medical Retailers
524,317 units affected
Recalled
Feb 5, 2026
Added
Mar 21, 2026
Coloplast Manufacturing US
Medium Risk
FDA Device
Coloplast Folysil and X-Flow Catheters Recalled for Sterility Issues
Distributed nationwide
Sold at medical supply distributors, hospitals +1 more
262,821 units affected
Recalled
Jan 10, 2025
Added
Mar 21, 2026
Maquet Cardiovascular
Medium Risk
FDA Device
Maquet Cardiovascular, LLC: Vasoview Hemopro Vessel Harvesting Systems Recalled for Component Failure
Distributed nationwide
Sold at Hospital suppliers, Medical device distributors
Recalled
Jul 11, 2024
Added
Mar 21, 2026
Boston Scientific
Critical Risk
FDA Device
Boston Scientific POLARx Balloon Catheters Recalled for Esophageal Fistula Risk
Distributed nationwide
Sold at Hospitals, Medical specialty distributors
35,739 units affected
Recalled
Nov 12, 2024
Added
Mar 21, 2026
Cardinal Health 200
Medium Risk
FDA Device
Cardinal Health 200, LLC: Jackson-Pratt 3-Spring Reservoir Kits Recalled for Lack of Sterilization
Distributed nationwide
Sold at Direct distribution, Healthcare facilities
Recalled
May 1, 2024
Added
Mar 21, 2026
Critical Risk
FDA Device
Medline Integrated Arterial Catheter Kits Recalled for Catheter Hub Defect
Distributed nationwide
Sold at Medline Industries, LP
Recalled
Jan 29, 2025
Added
Mar 21, 2026
Getinge Usa Sales
Medium Risk
FDA Device
Getinge Usa Sales Inc: Maquet Operating Room Light Systems Recalled Due to Risk of Falling
Distributed nationwide
Sold at Authorized Getinge Distributors, Medical Equipment Suppliers
236,793 units affected
Recalled
Jan 19, 2024
Added
Mar 21, 2026
Northeast Scientific
Medium Risk
FDA Device
NES Reprocessed Laser Atherectomy Catheters Recalled for Sterile Packaging Breach
Sold in 17 states
Sold at Hospitals, Surgical Centers +1 more
Recalled
Oct 2, 2025
Added
Mar 21, 2026
Abiomed
High Risk
FDA Device
Abiomed, Inc.: Introducer Kits Recalled for Pouch Holes and Sterility Loss Risk
Distributed nationwide
Sold at Hospitals, Medical Supply Distributors
Micro-organisms contamination
Recalled
Jan 5, 2024
Added
Mar 21, 2026
Intuitive Surgical
Medium Risk
FDA Device
da Vinci SP Access Port Kits Recalled for Potential Sterility Breach
Sold in 38 states
Sold at Authorized Medical Distributors, Intuitive Surgical, Inc.
41,526 units affected
Recalled
Jan 15, 2026
Added
Mar 21, 2026
Integra LifeSciences
High Risk
FDA Device
Integra LifeSciences Corp.: Cranial Access Kits Recalled Due to Potential Loss of Sterility
Distributed nationwide
Sold at Integra LifeSciences Corp., Medical distributors
17,753 units affected
Recalled
Feb 28, 2024
Added
Mar 21, 2026
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