Medisound, Inc./Digital Radiology Center, in Kissimmee, Florida Performing Mammography Without an MQSA Certificate
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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.
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08/16/12
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Narrowed Indications for Use for the Stryker Wingspan Stent System
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08/08/12
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UPDATE on Advanced Sterilization Products (ASP) Sterrad Cyclesure 24 Biological Indicators Revised Expiration Dates
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07/06/12
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Catheter Entrapment with the ev3 Onyx Liquid Embolic System
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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
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06/08/12
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FDA, NIOSH and OSHA Joint Safety Communication: Blunt-Tip Surgical Suture Needles Reduce Needlestick Injuries and the Risk of Subsequent Bloodborne Pathogen Transmission to Surgical Personnel
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05/30/12
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Dialysate Concentrates and Alkali Dosing Errors with Hemodialysis
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05/25/12
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Chronic Cerebrospinal Venous Insufficiency Treatment in Multiple Sclerosis Patients
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05/10/12
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Choking Hazard and Serious Injuries with the Spinbrush line of Powered Toothbrushes
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02/16/12
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Illegal Sale of Potentially Unsafe Hand-held Dental X-Ray Units
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02/10/12
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UPDATE on Life-Threatening Injuries Associated with the ShoulderFlex Massager
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12/21/11
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FDA Updated Communication on Use of Jet Injectors with Inactivated Influenza Vaccines
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10/21/11
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Preventing Surgical Fires
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10/13/11
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FDA Safety Communication: Life-Threatening Injuries Associated with the ShoulderFlex Massager
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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
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07/13/11
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Breast Cancer Screening - Thermography is Not an Alternative to Mammography
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06/02/11
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FDA and HRSA Joint Safety Communication: Weck Hem-o-Lok Ligating Clips Contraindicated for Ligation of Renal Artery During Laparoscopic Living-Donor Nephrectomy
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05/05/11
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UPDATE on Serious Complications Associated with Negative Pressure Wound Therapy Systems
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02/24/11
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Reports of Anaplastic Large Cell Lymphoma (ALCL) in Women with Breast Implants
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01/26/11
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Questions and Answers About the Abbott Glucose Test Strip Recall
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12/22/10
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Risk of Eye and Skin Injuries from High-powered, Hand-held Lasers Used for Pointing or Entertainment
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12/16/10
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Use of Fingerstick Devices on More Than One Person Poses Risk for Transmitting Bloodborne Pathogens: Initial Communication: Update 11/29/2010
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11/29/10
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Safety Investigation of CT Brain Perfusion Scans: Update 11/9/2010
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11/09/10
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Safety Investigation of Non-Coring (Huber) Needles: Updated October 25, 2010
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10/25/10
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CPSC and FDA Warn Against Using Infant Sleep Positioners Because of Suffocation Risk: Initial Communication
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09/29/10
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Safety Investigation of Patient Burns Associated with Electric Dental Handpieces and Electric Oral Bone-cutting Handpieces
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09/23/10
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Mammography Problems at Medisound, Inc. in Kissimmee, Florida
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08/27/10
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Information about Huber Needles
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08/26/10
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Ultraviolet Radiation Over-Exposure from Tootsie Tanner, a Portable Foot Tanning Device
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08/20/10
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Mammography Problems at Med Pro Imaging in Plantation, Florida
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08/17/10
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Positive Displacement Needleless Connectors and Bloodstream Infections: Initial Communication
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08/11/10
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Safety Investigation of Suspected Counterfeit Combat Application Tourniquets (C-A-T®): Initial Communication
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08/09/10
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Removing Retrievable Inferior Vena Cava Filters: Initial Communication
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08/09/10
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Letter to Infection Control Practitioners Regarding Positive Displacement Needleless Connectors
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07/28/10
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FDA's Final Order to Baxter to Recall, Refund, or Replace the Colleague Infusion Pumps
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07/13/10
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Questions and Answers About the Baxter Colleague Recall, Refund, and Replacement Action
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07/13/10
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FDA Safety Notification: Risk of Air or Gas Embolism When Using Air- or Gas- Pressurized Spray Devices
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07/09/10
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Class I Recall and Safety Investigation of Counterfeit Polypropylene Surgical Mesh: Updated June 10, 2010
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06/10/10
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Defective Cardiac Science Corporation Powerheart, CardioVive, Nihon Kohden, and GE Responder External Defibrillators: Updated July 19, 2010
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04/27/10
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Recalls of Q-Syte™ Luer Access Split Septum and Products Containing the Q-Syte™ Luer Access Split Septum: Initial Communication
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03/17/10
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Information About STERIS System 1
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02/22/10
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Preventing Cross-Contamination in Endoscope Processing
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11/19/09
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Energy Levels in External Biphasic Defibrillators: Initial Communication
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11/05/09
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Reminder from FDA: Cybersecurity for Networked Medical Devices is a Shared Responsibility
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11/04/09
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Safety Investigation of Certain Medical Device Power Cords: Initial Communication
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10/19/09
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Philips Lifeline Personal Help Button
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09/21/09
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Philips Avalon Fetal Monitors
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09/04/09
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Ongoing Safety Review of Arthroscopic Shavers
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07/06/09
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Surgical Mesh
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10/21/08
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Boston Scientific / Guidant Recall: Questions & Answers (April 10, 2007)
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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
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11/07/03
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MRI Safety
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09/18/01
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