Goldenberg Lauricella PLLC
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Blog

Camp Lejeune Lawsuits Receive National Spotlight

Tuesday December 6th, 2022 Firm News, News

Free Consultations With over 14,000 claims already filed and thousands more coming, the Camp Lejeune litigation is expected to be one of the largest mass litigations in history. A recent CBS report has cast a light on one of the many stories of individuals seeking justice for injuries suffered from exposure to toxic water…

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How Do Medications Become Contaminated?

Sunday October 9th, 2022 Defective Products, Firm News

It is no secret that pharmaceutical companies have been in the news for all the wrong reasons lately. From employee errors to lack of supervision, the dangers of pharmaceutical contamination are real and should not be taken lightly. Despite this, many individuals continue to take their prescription medications without a second thought. But what…

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What You Need to Know About Defective Products

Monday September 12th, 2022 Defective Products, Firm News

What is a Defective Product? A defective product is any product that is not safe for its intended use. This can include everything from a toy with small parts that pose a choking hazard to a car with faulty brakes. If a product is defective, it can cause serious injuries or even death. Who is Responsible…

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Flow-c and Flow-e Anesthesia Systems Recalled

Wednesday September 7th, 2022 Defective Medical Devices, Firm News

If you or a loved one experienced breathing or blockage issues during a surgical procedure due to a faulty suction unit, you may have a case against the manufacturer. In May 2022, Getinge USA Sales Inc. recalled Flow-c and Flow-e Anesthesia Systems due to reports of cracked or broken suction system power switches. The U.S….

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Smiths Medical Recalls Medfusion 3500 and 4000 Syringe Infusion Pumps Due to Software Malfunctions

Wednesday August 31st, 2022 Defective Medical Devices, Firm News

If you or a loved one suffered an injury during surgery or a hospital stay due to improper or delayed dosing from a malfunctioning syringe pump, you may have a case against the manufacturer. In April 2022, Smiths Medical recalled Medfusion 3500 and 4000 Syringe Infusion Pumps due to software malfunctions that can impact infusion delivery. 118,055…

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Medtronic HeartWare Ventricular Assist Device (HVAD) System Recall

Wednesday August 17th, 2022 Defective Medical Devices, Firm News

For more than a year, Medtronic’s HeartWare Ventricular Assist Device (HVAD) breathing systems have faced an onslaught of recalls due to severe issues that can cause serious injury or even death to patients. Medtronic’s HVAD systems were regularly implanted in patients with severe heart failure to help pump blood from the heart to the rest of…

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Recent Posts

  • Record-Setting Medical Malpractice Verdict Obtained by Goldenberg Lauricella for Wisconsin Child’s Family
  • Blue Ox SwayPro Injuries
  • RECALL: Zicam and Orajel Swabs Pulled from Shelves Due to Fungal Contamination
  • Igloo Recalls Over 1.2 Million Coolers Due to Fingertip Amputation and Crushing Risks
  • FDA Issues PowerPICC Catheter Warning Amid Surge in Bard PowerPort Lawsuits

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Goldenberg Lauricella PLLC
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