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Hamiton Medical issued a letter to affected customers regarding updated use instructions for certain coaxial breathing circuit sets used with HAMILTON...
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Urgent Care,
- Critical Access Hospitals,
- Hospitals,
- Office-Based Surgery
The Food and Drug Administration (FDA) has been notified that BD (Becton, Dickinson and Company) is voluntarily recalling lot 4032183 of ChloraPr...
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Assisted Living,
- Urgent Care,
- Dialysis Facilities,
- Medical Office,
- Critical Access Hospitals,
- Home Health,
- Hospitals,
- Long Term Care,
- Ambulatory Care,
- Office-Based Surgery,
- Inpatient Rehabilitation Facility,
- Clinical Lab,
- Pharmacy,
- Hospice,
- Rural Health Clinics
CMS released educational materials in support of the Medicare GLP-1 Bridge, which will start on July 1, 2026. Through this short-term demonstrati...
- Centers for Medicare and Medicaid Services
- Telehealth,
- Medical Office,
- Critical Access Hospitals,
- Hospitals,
- Ambulatory Care,
- Pharmacy,
- Rural Health Clinics
GE HealthCare has issued a letter to affected customers recommending Infant Resuscitation Systems and Warmers with a M1091607-R blender be corrected p...
- Food and Drug Administration
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals
Becton Dickinson & Company has issued a letter to affected customers recommending all anesthesia trays be corrected prior to continued use by remo...
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals,
- Ambulatory Care
The FDA has updated the “Hintermann Series H3 Total Ankle Replacement System and Long-Term Risk of Device Failure” Safety Communication to...
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Critical Access Hospitals,
- Hospitals,
- Ambulatory Care
Abiomed has issued a letter to affected customers recommending all 14Fr Low Profile Introducer Kits be removed from where they are used or sold. Ab...
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals
The FDA is aware that KayserBetten has issued a letter to affected customers recommending all KayserBett IDA pediatric care beds be corrected prior to...
- Food and Drug Administration
- Critical Access Hospitals,
- Home Health,
- Hospitals
Erbe USA has issued a letter to affected customers recommending certain Erbe Flexible Cryoprobes be removed from where they are used or sold. ...
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals,
- Ambulatory Care,
- Rural Health Clinics
The FDA has updated the Ventilator Correction: Philips Issues Correction for Trilogy Evo Platform Ventilators recall communication as Philips has clar...
- Food and Drug Administration
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals,
- Long Term Care
Insulet Corporation, Inc. announced a voluntary Medical Device Correction for specific lots of Omnipod® 5, Omnipod DASH®, and Omnipod® Ins...
- Food and Drug Administration
- All Healthcare Organizations
In the Federal Independent Dispute Resolution (IDR) Operations final rules released today, the Departments of Health and Human Services, Labor, and Tr...
- U.S. Department of Health and Human Services (HHS),
- Centers for Medicare and Medicaid Services
- All Healthcare Organizations
The FDA is aware that ICU Medical has issued a customer communication recommending certain IV tubing sets be removed from where they are used or sold....
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Urgent Care,
- Dialysis Facilities,
- Medical Office,
- Critical Access Hospitals,
- Home Health,
- Hospitals,
- Long Term Care,
- Ambulatory Care,
- Inpatient Rehabilitation Facility,
- Behavioral Health - Inpatient,
- Hospice,
- Rural Health Clinics
Medline has issued a letter to affected customers recommending certain Namic Manifolds be removed from where they are used or sold. Affected devices: ...
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals,
- Ambulatory Care
The FDA is aware that Abiomed has issued an Urgent Medical Device Recall (Correction) notice to affected customers recommending updated use instructio...
- Food and Drug Administration
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals