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Diagnostic Equipment
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Implants & Prosthetics
(230)
Monitoring Devices
(252)
Diagnostic Equipment
(818)
Home Healthcare
(215)
Contact Lenses & Vision
(17)
Surgical Equipment
(896)
818 recalls
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Remel
Medium Risk
FDA Device
Zebra Thermal Barcode Printers Recalled for Fire and Overheating Hazard
Sold in 17 states
Sold at Authorized distributors, Direct sales to medical facilities
Recalled
Mar 19, 2025
Added
Mar 21, 2026
CHANGE HEALTHCARE CANADA
Medium Risk
FDA Device
CHANGE HEALTHCARE CANADA COMPANY: Stratus Imaging PACS and Share Recalled for Incorrect Patient Data Association
Distributed nationwide
Sold at Authorized distributors, Direct sales to healthcare facilities
Recalled
Dec 14, 2023
Added
Mar 21, 2026
Electro Medical Systems SA
Medium Risk
FDA Device
Electro Medical Systems SA: Dental Cleaning and Water Bottles Recalled Due to Pressurized Detachment Risk
Sold in Illinois, Texas
Sold at Authorized EMS Dental distributors, Specialty dental suppliers
Complaints received regarding disassembly under pressure; no specific injury counts provided.
Recalled
Apr 24, 2024
Added
Mar 21, 2026
Vyaire Medical
Critical Risk
FDA Device
Vyaire Medical, Inc.: Vyaire Twin Tube Sample Lines Recalled for Nozzle Separation Risk
Distributed nationwide
Sold at Vyaire Medical, Inc.
Recalled
May 8, 2024
Added
Mar 21, 2026
EVIDENT SCIENTIFIC
Medium Risk
FDA Device
EVIDENT SCIENTIFIC INC: SlideView VS200 Slide Viewer Recalled Due to Shutter and Laser Malfunction
Distributed nationwide
Sold at authorized medical device distributors
Recalled
Jul 26, 2024
Added
Mar 21, 2026
Medium Risk
FDA Device
Siemens Medical Solutions USA, Inc: Siemens X-Ray Systems Recalled for Falling Support Arm Risk
Distributed nationwide
Sold at Siemens Medical Solutions USA, Inc.
Recalled
Aug 7, 2024
Added
Mar 21, 2026
Ortho-Clinical Diagnostics
Medium Risk
FDA Device
Ortho-Clinical Diagnostics, Inc.: VITROS Systems Recalled Due to Software Defect and Incorrect Patient Results
Sold in 21 states
Sold at Ortho-Clinical Diagnostics, Inc., Professional medical distributors
Recalled
Mar 1, 2024
Added
Mar 21, 2026
Philips North America
Critical Risk
FDA Device
Philips North America Llc: Panorama 1.0T HFO MR Systems Recalled for Potential Gas Pressure Buildup
Sold in 34 states
Sold at Authorized medical device distributors, Direct sales to healthcare facilities
Helium gas contamination
Recalled
Dec 14, 2023
Added
Mar 21, 2026
Philips North America
Medium Risk
FDA Device
Philips North America: BrightView Gamma Camera Systems Recalled for Entrapment Hazard
Distributed nationwide
Sold at Authorized Medical Equipment Distributors, Direct Sales to Medical Facilities
Recalled
Jan 5, 2024
Added
Mar 21, 2026
Orthoscan
Medium Risk
FDA Device
Ziehm Mobile C-arm X-ray Systems Recalled for Unintended Radiation Risk
Distributed nationwide
Sold at authorized medical equipment distributors, Ziehm Imaging, Inc.
Recalled
Dec 2, 2024
Added
Mar 21, 2026
Philips North America
Medium Risk
FDA Device
Philips North America: ProxiDiagnost N90 Systems Recalled for Image Mixing and Security Vulnerability
Distributed nationwide
Sold at Authorized Medical Distributors, Direct Medical Sales
Recalled
Feb 9, 2024
Added
Mar 21, 2026
Ortho-Clinical Diagnostics
Medium Risk
FDA Device
VITROS Chemistry CRP Slides Recalled for Incorrect Labeling
Sold in 29 states
Sold at Authorized medical distributors
Recalled
May 29, 2025
Added
Mar 21, 2026
Microbiologics
Medium Risk
FDA Device
Microbiologics KWIK-STIK and LYFO DISK Recalled for Testing Failure
Distributed nationwide
Sold at Laboratory distributors, Microbiologics Inc
Campylobacter jejuni subsp. jejuni contamination
Recalled
Dec 22, 2025
Added
Mar 21, 2026
GE Hangwei Medical Systems
High Risk
FDA Device
GE Hangwei Medical Systems, Co. LTD: Definium Tempo X-Ray Systems Recalled for Falling Hazard
Distributed nationwide
Sold at GE HealthCare Authorized Dealers
Recalled
Dec 14, 2023
Added
Mar 21, 2026
Philips Healthcare
Medium Risk
FDA Device
Philips Healthcare: Incisive CT Systems Recalled for Software-Related Scan Inaccuracy
Distributed nationwide
Sold at Philips Healthcare
Recalled
Sep 30, 2023
Added
Mar 21, 2026
Medium Risk
FDA Device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Allura Xper and Azurion X-ray Systems Recalled for Monitor Image Defects
Distributed nationwide
Sold at Authorized Philips medical equipment distributors, Direct B2B sales to hospitals and clinics
Recalled
Feb 16, 2024
Added
Mar 21, 2026
Medium Risk
FDA Device
Philips Azurion Image-Guided Therapy Systems Recalled for Unexpected Movement
Distributed nationwide
Sold at Philips Medical Systems, Medical device distributors
11,614 units affected
Recalled
Feb 11, 2026
Added
Mar 21, 2026
GE Medical Systems
Medium Risk
FDA Device
GE HealthCare X-Ray Systems Recalled for Automatic Exposure Control Safety Issue
Distributed nationwide
Sold at Authorized Medical Equipment Distributors, GE HealthCare Direct
Recalled
Feb 3, 2025
Added
Mar 21, 2026
High Risk
FDA Device
Olympus Corporation of the Americas: Water Filters Recalled Due to Assembly Error and Infection Risk
Distributed nationwide
Sold at Olympus Corporation of the Americas
Unfiltered tap water contamination
Recalled
Feb 7, 2024
Added
Mar 21, 2026
Baxter Healthcare
Medium Risk
FDA Device
Baxter Healthcare Corporation: Welch Allyn CP150 Electrocardiograph Recalled for Missing EMI Component
Sold in Illinois
Sold at Authorized medical distributors
Recalled
Jul 10, 2024
Added
Mar 21, 2026
GE Medical Systems
Medium Risk
FDA Device
GE LOGIQ P9 and P10 Ultrasound Systems Recalled for Inaccurate Measurements
Distributed nationwide
Sold at Authorized medical device distributors, GE Healthcare Sales
Recalled
Oct 15, 2025
Added
Mar 21, 2026
Instrumentation Laboratory
Medium Risk
FDA Device
Instrumentation Laboratory: GEM Premier 3000 PAK Cartridges Recalled for Inaccurate Oxygen Readings
Sold in Massachusetts, Minnesota, New York
Sold at Authorized Medical Distributors, Hospitals +1 more
Recalled
Nov 21, 2023
Added
Mar 21, 2026
Cepheid
Medium Risk
FDA Device
Cepheid: Sample Collection Device Recalled for Potential Biohazard Leakage
Sold in 51 states
Sold at Authorized distributors, Healthcare facilities
Biohazard exposure contamination
Recalled
Aug 14, 2024
Added
Mar 21, 2026
Medium Risk
FDA Device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Azurion Fluoroscopic X-ray Systems Recalled for Loss of Imaging Functionality
Distributed nationwide
Sold at Philips Medical Systems, authorized medical equipment distributors
Recalled
Aug 8, 2024
Added
Mar 21, 2026
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