Tag Archives: Medical Device Recall
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LIFEPAK 1000 Defibrillators May Shut Down During Use, FDA Warns
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3M Claims False Bair Hugger Recall Rumors Being Spread By Competitor
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Zimmer Biomet Shoulder Recall Issued Amid High Fracture Rate
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Duodenoscope Recall Issued by Fujifilm For Older Models Linked To Infection Risk
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Nurse Assist Flush Syringe Recall Classified Class I By FDA Over Infection Risks
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Top 10 Recalls from 2016
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Hip Replacement Surgical Device Recalled Due Amid Sterilization Concerns
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FDA Issues New Guidance On When To Warn Public About Medical Device Problems
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Bacterial Infection Outbreak at Nursing Homes and Hospitals Linked To Contaminated Syringes