Go Backs

Diagnostic Equipment

AllImplants & Prosthetics(226)Monitoring Devices(263)Diagnostic Equipment(818)Home Healthcare(223)Contact Lenses & Vision(17)Surgical Equipment(895)

818 recalls

per page
Noah Medical
Medium RiskFDA Device

Galaxy System Recalled for Password-Protected User Manual

  • Sold in 20 states
  • Sold at Authorized distributors, Noah Medical Corporation direct sales
Recalled
Added
Philips North America
Medium RiskFDA Device

Philips Spectral CT Systems Recalled for Unintended Gantry and Table Motion

  • Sold in 19 states
  • Sold at Authorized medical device distributors, Direct sales from Philips North America Llc
Recalled
Added
DRG International
Low RiskFDA Device

DRG 17-OH Progesterone ELISA Test Kits Recalled for Labeling Error

  • Sold in Arizona, California, New Hampshire
  • Sold at Direct distribution
Recalled
Added
Bio-Rad Laboratories
Medium RiskFDA Device

Bio-Rad Laboratories: QXDx BCR-ABL %IS Kit Recalled for Potential Incorrect Results

  • Sold in 5 states
  • Sold at Laboratory distributors
Recalled
Added
Philips North America
Medium RiskFDA Device

Philips North America: Spectral CT on Rails Recalled for Potential Gantry Collisions

  • Sold in Minnesota
Recalled
Added
DRG International
Low RiskFDA Device

DRG International, Inc.: Salivary Testosterone ELISA Kits Recalled for Invalid Test Results

  • Sold in 6 states
Recalled
Added
RAYSEARCH LABORATORIES AB
Medium RiskFDA Device

RayStation Radiation Therapy Software Recalled for Incorrect Dose Calculations

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Direct Sales from RaySearch Laboratories
Recalled
Added
GE Medical Systems China
Medium RiskFDA Device

GE Versana and LOGIQ Ultrasound Systems Recalled for Fetal Measurement Errors

  • Distributed nationwide
  • Sold at GE HealthCare authorized distributors, Specialty medical equipment retailers
Recalled
Added
Medium RiskFDA Device

Abbott, BD, and Ortho Diagnostic Tests Recalled for Temperature Issues

  • Sold in 11 states
  • Sold at McKesson Medical-Surgical Inc.
Recalled
Added
Philips North America
Medium RiskFDA Device

Philips MR Systems Recalled for Potential Errors in MRE Stiffness Maps

  • Sold in 20 states
  • Sold at Authorized Philips medical device distributors
Recalled
Added
Philips North America
Medium RiskFDA Device

Philips North America Llc: HA FlexTrak Patient Trolleys Recalled Due to Potential Oil Leaks and Slip Hazard

  • Distributed nationwide
  • Sold at Authorized Philips medical device distributors, Direct sales to hospitals and clinics
Recalled
Added
WASATCH PHOTONICS
Medium RiskFDA Device

Wasatch Photonics Raman Spectrometers Recalled for Laser Safety Failure Risks

  • Distributed nationwide
  • Sold at Wasatch Photonics, Authorized distributors
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: EVIS EXERA III Video System Centers Recalled for Power Supply Failures

  • Distributed nationwide
  • Sold at Olympus Corporation of the Americas
Recalled
Added
Instrumentation Laboratory
Low RiskFDA Device

HemosIL SynthAFax Laboratory Tests Recalled for Excess Preservative

  • Sold in 4 states
  • Sold at Laboratory suppliers, Medical distributors
Recalled
Added
Philips Ultrasound
Low RiskFDA Device

Philips Ultrasound, Inc: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  • 171,322 units affected
Recalled
Added
Beckman Coulter Ireland
Low RiskFDA Device

Apo B Reagent Recalled for Potential Incorrect Patient Test Results

  • Sold in 19 states
  • Sold at Authorized distributors, Medical supply channels
Recalled
Added
Philips Medical Systems DMC
Medium RiskFDA Device

Philips Diagnostic Systems Recalled for Vertical Movement Defect

  • Distributed nationwide
  • Sold at Philips direct sales, authorized medical device distributors
Recalled
Added
Philips North America
Medium RiskFDA Device

Philips North America: Quadrature Body Coil (QBC) Recalled for Sharp Edges and Seal Failure

  • Distributed nationwide
  • Sold at medical equipment distributors, Philips direct sales
Recalled
Added
Young Dental Manufacturing I
Medium RiskFDA Device

Young Dental Manufacturing I, LLC: Biotrol Purit Clean-It Ultrasonic Cleaner Recalled for Bacterial Contamination

  • Sold in 10 states
  • Sold at Authorized distributors
  • Bacteria contamination
Recalled
Added
GE Medical Systems
Medium RiskFDA Device

GE Medical Systems, LLC: OEC Elite and OEC 3D Mobile C-Arms Recalled for Excessive X-ray Exposure

  • Distributed nationwide
  • Sold at Authorized GE Medical Systems distributors, Medical device supply channels
Recalled
Added
Advance Medical Designs
Medium RiskFDA Device

Advance Medical Designs, Inc.: Ultrasound Gel and Procedural Kits Recalled for Mislabeled Inappropriate Use

  • Distributed nationwide
  • Sold at Advance Medical Designs, Inc., Medical Supply Distributors
  • 160,865 units affected
Recalled
Added
Philips North America
Medium RiskFDA Device

Philips MR Systems Recalled for Gradient Coil Component Fire Risk

  • Distributed nationwide
  • Sold at hospitals, imaging centers +1 more
Recalled
Added
GE Healthcare
Medium RiskFDA Device

GE Healthcare: Centricity PACS and Universal Viewer Software Recalled for Patient Data Mix-ups

  • Distributed nationwide
  • Sold at Authorized GE HealthCare medical device distributors, Direct sales to hospitals and clinics
Recalled
Added
Abbott
Medium RiskFDA Device

Abbott GmbH: Anti-HCV Reagent Kits Recalled for Falsely Elevated Patient Results

  • Distributed nationwide
  • Sold at Abbott GmbH, Medical laboratories +1 more
  • 12,329 units affected
Recalled
Added