Go Backs

Diagnostic Equipment

AllImplants & Prosthetics(226)Monitoring Devices(267)Diagnostic Equipment(820)Home Healthcare(229)Contact Lenses & Vision(17)Surgical Equipment(891)

820 recalls

per page
Philips Ultrasound
Medium RiskFDA Device

Philips Ultrasound Transducers Recalled for Refurbishment Beyond Useful Life

  • Distributed nationwide
  • Sold at Authorized Medical Equipment Distributors, Healthcare Facilities
Recalled
Added
Medium RiskFDA Device

Philips IntelliSpace Cardiovascular Software Recalled for Missing Report Data

  • Distributed nationwide
  • Sold at Direct sales to healthcare facilities, Authorized Philips medical distributors
Recalled
Added
Beckman Coulter Mishima K.K.
Medium RiskFDA Device

Beckman Coulter Mishima K.K.: DxC 500 AU Clinical Chemistry Analyzer Recalled for Software Bug

  • Sold in 13 states
  • Sold at Beckman Coulter, Medical laboratories +1 more
Recalled
Added
Medium RiskFDA Device

Olympus Corporation of the Americas: Gastrointestinal Videoscopes Recalled for Inadequate Sterilization Drying Time

  • Distributed nationwide
  • Sold at Olympus Corporation of the Americas
Recalled
Added
Medium RiskFDA Device

Siemens Healthcare Diagnostics, Inc.: CA 19-9 Diagnostic Test Kits Recalled for Inaccurate Test Results

  • Distributed nationwide
  • Sold at Medical distributors, Siemens Healthcare Diagnostics
Recalled
Added
Medium RiskFDA Device

Siemens Medical Solutions USA, Inc: Sensis Vibe Hemo Recalled Due to Potential Application Crashes

  • Sold in California, Connecticut, Florida
  • Sold at Siemens Medical Solutions USA, Inc
Recalled
Added
Alere San Diego
Medium RiskFDA Device

Alere San Diego, Inc.: Cholestech LDX Battery Kits Recalled Due to Swelling and Burn Risks

  • Distributed nationwide
  • Sold at Authorized distributors
Recalled
Added
Cepheid
Medium RiskFDA Device

Cepheid Xpert BCR-ABL Ultra Test Kits Recalled for Inaccurate Results

  • Sold in 29 states
  • Sold at Laboratory suppliers, Medical device distributors
  • 10,357 units affected
Recalled
Added
Diversatek Healthcare
Low RiskFDA Device

Zvu Anorectal Manometry Kits Recalled for Mislabeled Expiration Date

  • Sold in 4 states
  • Sold at Diversatek Healthcare
Recalled
Added
GE Medical Systems
Medium RiskFDA Device

GE MR Imaging Systems Recalled for Potential Caster Lock Failure

  • Distributed nationwide
  • Sold at GE HealthCare authorized distributors, Direct medical sales
Recalled
Added
PHILIPS MEDICAL SYSTEMS
Medium RiskFDA Device

Philips Incisive CT and CT 5300 Systems Recalled for Multiple Software Issues

  • Sold in 18 states
  • Sold at hospitals, medical clinics +1 more
Recalled
Added
Medline Industries
Medium RiskFDA Device

Medline Kits with Tego Connectors Recalled for Defective Silicone Seals

  • Distributed nationwide
  • Sold at Authorized distributors, Direct medical sales
  • Biological contaminants (risk of exposure due to damaged seals) contamination
Recalled
Added
Medium RiskFDA Device

SAFE-T-FILL Blood Gas Capillary Accessories Recalled for Quality Issues

  • Distributed nationwide
  • Sold at Medical distributors, Anatomy Supply Partners
  • 714,772 units affected
Recalled
Added
Vision RT
Medium RiskFDA Device

AlignRT InBore Systems Recalled for Missing Laser Safety Information

  • Distributed nationwide
  • Sold at Authorized medical device distributors
Recalled
Added
Philips North America
Medium RiskFDA Device

Philips North America Llc: Magnetic Resonance Systems Recalled for Incorrect Support Table Installation

  • Distributed nationwide
  • Sold at Philips authorized medical equipment distributors, specialized hospital supply chains
  • 10,221 units affected
Recalled
Added
Medium RiskFDA Device

Philips Medical Systems Quadrature Body Coils Recalled for Loose Seals

  • Distributed nationwide
  • Sold at Medical facilities, Authorized Philips medical distributors
Recalled
Added
LEICA BIOSYSTEMS NUSSLOCH
Medium RiskFDA Device

LEICA BIOSYSTEMS NUSSLOCH GMBH: Cryostats Recalled Due to Fire and Burn Risk from Flammable Freezing Sprays

  • Distributed nationwide
  • Sold at Authorized medical device distributors, Direct sales from Leica Biosystems
Recalled
Added
Guangzhou Pluslife Biotech
Medium RiskFDA Device

MiniDock Devices and Pluslife COVID-19 Test Kits Recalled for Lacking FDA Clearance

  • Distributed nationwide
  • Sold at Authorized distributors
Recalled
Added
Fujirebio Diagnostics
Medium RiskFDA Device

Lumipulse Alzheimer's Test Kits Recalled for Inaccurate Results

  • Sold in 13 states
  • Sold at Clinical laboratories, Medical facilities
Recalled
Added
Medium RiskFDA Device

FLEX CD20cy (Dako Omnis) Antibody Recalled for Potential False Negative Risk

  • Sold in 32 states
  • Sold at Authorized medical laboratory distributors, Agilent Technologies
Recalled
Added
Lucid Diagnostics
Medium RiskFDA Device

Lucid Diagnostics, Inc.: EsophaCap Sponges Recalled Due to Risk of Detachment During Removal

  • Sold in Minnesota, Maryland
  • Sold at Clinical sites, Distributors
Recalled
Added
Family Dollar Stores
Medium RiskFDA Device

Family Dollar Stores, Llc.: Various Health and Oral Care Products Recalled Due to Temperature Mismanagement

  • Sold in 23 states
  • Sold at Family Dollar
  • 329,044 units affected
Recalled
Added
Beckman Coulter
Medium RiskFDA Device

Beckman Coulter UIBC Assay Kits Recalled for Inaccurate Test Results

  • Sold in 9 states
  • Sold at Authorized Medical Distributors, Direct Sales to Laboratories
  • 56,696 units affected
Recalled
Added
GET TESTED INTERNATIONAL AB
Medium RiskFDA Device

Get Tested International Diagnostic Test Kits Recalled for Lack of FDA Clearance

  • Distributed nationwide
  • Sold at GET TESTED INTERNATIONAL AB
  • 25,201 units affected
Recalled
Added