Tag Archives: Medical Device Recall
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Seprafilm Recall Urged by Public Citizen, Indicating Side Effects Outweigh Benefits
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Flow-i Anesthesia Systems Recall Issued Over Possible Loss of Ventilation
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Tracheostomy Tube Recall Issued by Medtronic Following Reports of Problems, Injuries
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FDA Launches Medical Device Identification Site
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New Report Details Path To Better Medical Device Postmarketing Surveillance
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FDA To Require More Stringent Approval Process for Automated External Defibrillators
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Infant Hospital Pillow Recall Expanded Due to Risk of Mold on Gel-E-Donut, Squishon 2
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Medical Devices Often Lack Publicly Available Evidence of Safety, Effectiveness
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Mold Fears Lead to Gel-E-Donut and Squishon 2 Infant Pillow Recall