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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
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
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
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
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
FDA Medical Device Recall - Ventilator Recall: React Health Removes VOCSN V+Pro Ventilators
05/21/2026Ventec, doing business as React Health, has issued a letter to affected customers recommending certain VOCSN V+Pro units be removed fro...
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals,
- Long Term Care
CDC Health Advisory: Ebola Disease Outbreak in the Democratic Republic of the Congo and Uganda
05/20/2026The Centers for Disease Control and Prevention (CDC) has issued another Health Alert Network (HAN) Health Advisory to alert clinicians, public health ...
- Centers for Disease Control and Prevention
- All Healthcare Organizations
Relocating and Revising CMS Surveyor Guidance for End-Stage Renal Disease (ESRD) Facilities
05/20/2026The Centers for Medicare & Medicaid Services (CMS) is relocating the interpretive guidance and survey procedures to Appendix H of the State Operat...
- Centers for Medicare and Medicaid Services
- Rural Emergency Hospitals,
- Dialysis Facilities,
- Critical Access Hospitals,
- Hospitals,
- Long Term Care,
- Ambulatory Care
The FDA updated its medical device recall listing on 2026-05-18 for Draeger, Inc.’s Atlan A350 and Atlan A350 XL anesthesia workstations, which ...
- Food and Drug Administration
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals,
- Long Term Care
The CDC has issued updates related to the Ebola outbreak in the Democratic Republic of the Congo (DRC) and Uganda. The WHO followed this notifica...
- Centers for Disease Control and Prevention
- All Healthcare Organizations