Go Backs

Nationwide Recalls

12,561 recalls distributed in Nationwide

per page
United Pharmacy
Medium RiskFDA Drug

United Pharmacy: Glutamine, Arginine and Carnitine Injection Recalled for Impurities

  • Distributed nationwide
  • Sold at United Pharmacy
  • unknown impurities contamination
Recalled
Added
Hologic
Medium RiskFDA Device

Hologic Sizer Set Sterilization Trays Recalled for Incorrect Instructions

  • Distributed nationwide
  • Sold at Authorized Medical Distributors
Recalled
Added
Medium RiskFDA Device

HotDog and Hillrom Temperature Controllers Recalled for System Power Errors

  • Distributed nationwide
  • Sold at Augustine Surgical Inc., Hillrom +1 more
Recalled
Added
Beckman Coulter
Medium RiskFDA Device

Beckman Coulter DxI 9000 Analyzers Recalled for Software Error

  • Distributed nationwide
  • Sold at Direct Sales, Medical Equipment Distributors
Recalled
Added
Stryker
Medium RiskFDA Device

Stryker iBur Medical Devices Recalled for Potential Thermal Injury Risk

  • Distributed nationwide
  • Sold at Stryker Corporation authorized distributors, Direct medical sales channels
  • 23,330 units affected
Recalled
Added
Medium RiskFDA Device

PTS Diagnostics A1CNow+ HbA1c System Recalled for Inaccurate Test Results

  • Distributed nationwide
  • Sold at authorized dealers, medical distributors
Recalled
Added
Landauer
Medium RiskFDA Device

Landauer: microSTARii Readers Recalled Due to Dosimeter Measurement Inaccuracies

  • Distributed nationwide
  • Sold at Direct distribution
Recalled
Added
Landauer
Medium RiskFDA Device

Landauer: microSTARii Dosimetry Systems Recalled for Removal of Medical Use References

  • Distributed nationwide
  • Sold at Authorized medical device distributors, Landauer
Recalled
Added
Landauer
Medium RiskFDA Device

Landauer: nanoDot Radiation Dosimeters Recalled for Accuracy Issues

  • Distributed nationwide
  • Sold at Landauer, authorized medical device distributors
  • 1,678,258 units affected
Recalled
Added
Accuray
High RiskFDA Device

Accuray CyberKnife Treatment Systems Recalled for Mechanical Failure Risk

  • Distributed nationwide
  • Sold at authorized medical device distributors, specialty healthcare systems
Recalled
Added
Medtronic Neuromodulation
Medium RiskFDA Device

Medtronic Neuromodulation: Restore Clinician Programmer Software Recalled for Communication Failure

  • Distributed nationwide
  • Sold at Government distribution, Military distribution +1 more
Recalled
Added
Nuwellis
Critical RiskFDA Device

Nuwellis AquaFlexFlow UF 500 Plus Recalled for Fluid Imbalance Risk

  • Distributed nationwide
  • Sold at Hospital suppliers, Medical device distributors
Recalled
Added
DATEX--OHMEDA
Critical RiskFDA Device

GE Healthcare Giraffe Omnibeds and Incubators Recalled for Formaldehyde Risk

  • Distributed nationwide
  • Sold at Hospital supply channels, Direct medical distribution
  • Formaldehyde contamination
Recalled
Added
Philips Ultrasound
Medium RiskFDA Device

Philips EPIQ Ultrasound Systems Recalled for Reboot and Transducer Damage

  • Distributed nationwide
  • Sold at Philips Ultrasound, LLC
Recalled
Added
Genentech
Critical RiskFDA Drug

Genentech, Inc.: Activase (alteplase) Recalled for Potential Glass Contamination

  • Distributed nationwide
  • Sold at pharmacies, hospitals
  • Glass fragments contamination
Recalled
Added
Diamond Wipes International
Medium RiskFDA Drug

Diamond Wipes International, Inc.: Wet Wipes and Acne Towelettes Recalled for Poor Quality Manufacturing Water

  • Distributed nationwide
  • Sold at Better Planet Brands, Diamond Wipes Int'l, Inc.
  • 5,200,632 units affected
Recalled
Added
Teva Pharmaceuticals USA
Low RiskFDA Drug

Teva Pharmaceuticals USA: Lidocaine Patch 5% Recalled for Failed Stability Specifications

  • Distributed nationwide
  • Sold at pharmacies
  • 30,382 units affected
Recalled
Added
Ridge Properties
Medium RiskFDA Drug

Ridge Properties, LLC: Various Numbing Creams and Gels Recalled for Inadequate Manufacturing Controls

  • Distributed nationwide
  • Sold at NaturallyHL.com
Recalled
Added
Medium RiskFDA Drug

Avella of Deer Valley, Inc. Store 38: Bevacizumab Pre-filled Syringes Recalled for Lack of Sterility Assurance

  • Distributed nationwide
  • Sold at Avella Specialty Pharmacy
Recalled
Added
Zydus Pharmaceuticals USA
Medium RiskFDA Drug

Zydus Pharmaceuticals USA Inc: Paroxetine Tablets Recalled Due to Presence of Risperidone Tablets

  • Distributed nationwide
  • Sold at Pharmacies
  • Risperidone tablets contamination
Recalled
Added
Boiron
Low RiskFDA Drug

Boiron Inc.: Calendula Cream Recalled Due to Labeling Error on Ingredient Strength

  • Distributed nationwide
  • 52,810 units affected
Recalled
Added
Johnson Matthey
Low RiskFDA Drug

Johnson Matthey Inc.: Remifentanil HCl Active Ingredient Recalled for Unknown Impurities

  • Distributed nationwide
  • Sold at Pharmaceutical manufacturers, Retail pharmacies
  • Unknown impurity contamination
Recalled
Added
Pharmaceutical Associates
Low RiskFDA Drug

Pharmaceutical Associates Inc: Nystatin Oral Suspension Recalled for Appearance and Resuspension Issues

  • Distributed nationwide
  • Sold at Institutional Use Only
  • 275,400 units affected
Recalled
Added
PharMedium Services
Medium RiskFDA Drug

PharMedium Services, Llc: Fentanyl Citrate Recalled for Incorrect Expiration Date Labeling

  • Distributed nationwide
  • Sold at hospitals, clinics
Recalled
Added