- Alarm Fatigue Can Kill
- Freak Accidents Increase in Da Vinci Robot Surgery
- Johnson & Johnson Recalls Knee Device
- J&J Knew 40% of Hip Implants Would Fail
- Life Pulse Ventilator Circuits Recalled
- Zimmer Recalls PEEK Ardis Inserter Due to Death Risk
- Indoor Tanning Poses Significant Cancer Risk
- Hemorrhoid Surgical Stapler Recalled
- Resuscitators Recalled by Ventlab
- Senate Finds Medtronic Paid Docs to Manipulate InFuse Studies
- Software Bugs Put Critical Care Patients at Risk
- Symbiq Infusion Systems Recall
- J&J Recalls 157,000 Surgical Staplers
- FDA Warns Zimmer Over Hip Device
- Stryker’s Class 1 Recall: 1 Death Reported
- DePuy Recalls Faulty Custom Joint Implants
- FDA Recalls Another CareFusion Pump
- Mirena IUD Under Increased Scrutiny
- FDA Reprimands Medtronic Regarding Pumps
- Study: St. Jude Defibrillator Failures Persist
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