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UPDATED Laparoscopic Uterine Power Morcellation in Hysterectomy and Myomectomy: FDA Safety Communication
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11/24/14
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Adverse Events Associated with Use of Enhancement Medical's "Expression" Intranasal Splint as a Dermal Filler
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08/05/14
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Mammography Problems at Big Sky Diagnostic Imaging, LLC in Butte, Montana: FDA Safety Communication
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06/23/14
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Product Shortage of Advanced Sterilization Products Sterrad Cyclesure 24 Biological Indicator: FDA Safety Communication
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05/23/14
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Removing Retrievable Inferior Vena Cava Filters: FDA Safety Communication
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05/07/14
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Shasta Technologies GenStrip Blood Glucose Test Strips May Report False Results: FDA Safety Communication
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04/29/14
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Laparoscopic Uterine Power Morcellation in Hysterectomy and Myomectomy: FDA Safety Communication [ARCHIVED]
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04/17/14
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Breast Cancer Screening - Nipple Aspirate Test Is Not An Alternative To Mammography: FDA Safety Communication
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12/12/13
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Philips HeartStart Automated External Defibrillators (AED): FDA Safety Communication
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12/03/13
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Rare Serious Erosion Events Associated with St. Jude Amplatzer Atrial Septal Occluder (ASO): FDA Safety Communication
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10/17/13
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Mammography Problems at San Sebastian X-Ray in San Sebastian, Puerto Rico: FDA Safety Communication
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06/27/13
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Cybersecurity for Medical Devices and Hospital Networks: FDA Safety Communication
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06/13/13
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Stolen Covidien Surgical Stapler Reloads: FDA Safety Communication
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05/07/13
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Damaged or Worn Covers for Medical Bed Mattresses Pose Risk of Contamination and Patient Infection: FDA Safety Communication
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04/19/13
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Neptune 1 Silver Waste Management System and Neptune 2 Ultra Waste Management System (Neptune 1 Silver and Neptune 2 Ultra): Updated FDA Safety Communication
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03/27/13
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Metal-on-Metal Hip Implants: FDA Safety Communication
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01/17/13
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UPDATE on Advanced Sterilization Products (ASP) Sterrad Cyclesure 24 Biological Indicators Revised Expiration Dates: FDA Safety Communication
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11/08/12
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Medisound, Inc./Digital Radiology Center, in Kissimmee, Florida Performing Mammography Without an MQSA Certificate: FDA Safety Communication
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09/28/12
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Premature Insulation Failure in Recalled Riata Implantable Cardioverter Defibrillator (ICD) Leads Manufactured by St. Jude Medical, Inc.: FDA Safety Communication
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08/16/12
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Narrowed Indications for Use for the Stryker Wingspan Stent System: FDA Safety Communication
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08/08/12
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Catheter Entrapment with the ev3 Onyx Liquid Embolic System: FDA Safety Communication
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06/28/12
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UPDATE on Bacteria Found in Other-Sonic Generic Ultrasound Transmission Gel Poses Risk of Infection: FDA Safety Communication
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06/08/12
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Blunt-Tip Surgical Suture Needles Reduce Needlestick Injuries and the Risk of Subsequent Bloodborne Pathogen Transmission to Surgical Personnel: FDA, NIOSH and OSHA Joint Safety Communication
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05/30/12
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Dialysate Concentrates and Alkali Dosing Errors with Hemodialysis: FDA Safety Communication
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05/25/12
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Chronic Cerebrospinal Venous Insufficiency Treatment in Multiple Sclerosis Patients: FDA Safety Communication
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05/10/12
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Choking Hazard and Serious Injuries with the Spinbrush line of Powered Toothbrushes: FDA Safety Communication
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02/16/12
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Illegal Sale of Potentially Unsafe Hand-held Dental X-Ray Units: FDA Safety Communication
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02/10/12
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UPDATE on Life-Threatening Injuries Associated with the ShoulderFlex Massager: FDA Safety Communication [ARCHIVED]
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12/21/11
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Use of Jet Injectors with Influenza Vaccines: FDA Safety Communication
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10/21/11
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Preventing Surgical Fires: FDA Safety Communication [ARCHIVED]
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10/13/11
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Life-Threatening Injuries Associated with the ShoulderFlex Massager: FDA Safety Communication [ARCHIVED]
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08/25/11
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UPDATE on Serious Complications Associated with Transvaginal Placement of Surgical Mesh for Pelvic Organ Prolapse: FDA Safety Communication [ARCHIVED]
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07/13/11
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Breast Cancer Screening - Thermography is Not an Alternative to Mammography: FDA Safety Communication [ARCHIVED]
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06/02/11
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Weck Hem-o-Lok Ligating Clips Contraindicated for Ligation of Renal Artery During Laparoscopic Living-Donor Nephrectomy: FDA and HRSA Joint Safety Communication [ARCHIVED]
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05/05/11
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UPDATE on Serious Complications Associated with Negative Pressure Wound Therapy Systems: FDA Safety Communication [ARCHIVED]
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02/24/11
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Reports of Anaplastic Large Cell Lymphoma (ALCL) in Women with Breast Implants: FDA Safety Communication [ARCHIVED]
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01/26/11
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Preventing Cross-Contamination in Endoscope Processing: FDA Safety Communication [ARCHIVED]
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11/19/09
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Energy Levels in External Biphasic Defibrillators: Initial FDA Safety Communication [ARCHIVED]
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11/05/09
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Cybersecurity for Networked Medical Devices is a Shared Responsibility: FDA Safety Reminder [ARCHIVED]
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11/04/09
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Safety Investigation of Certain Medical Device Power Cords: Initial FDA Safety Communication [ARCHIVED]
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10/19/09
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Philips Lifeline Personal Help Button: FDA Safety Communication [ARCHIVED]
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09/21/09
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Philips Avalon Fetal Monitors: FDA Safety Communication [ARCHIVED]
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09/04/09
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Ongoing Safety Review of Arthroscopic Shavers: FDA Safety Communication [ARCHIVED]
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07/06/09
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Surgical Mesh: FDA Safety Communication [ARCHIVED]
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10/21/08
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Removing Retrievable Inferior Vena Cava Filters: FDA Safety Communication
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05/07/14
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Boston Scientific / Guidant Recall - Questions: FDA Safety Communication [ARCHIVED]
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04/10/07
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Laparoscopic Trocar Injuries: A report from a U.S. Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) Systematic Technology Assessment of Medical Products (STAMP) Committee: FDA Safety Communication [ARCHIVED]
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11/07/03
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MRI Safety: FDA Safety Communication [ARCHIVED]
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09/18/01
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