Goldenberg Lauricella PLLC
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Xeljanz Injuries: Major Adverse Cardiac Events

Friday March 12th, 2021 Dangerous Drugs, Defective Medical Devices, Firm News, Xeljanz

Xeljanz and MACE Injuries Preliminary results from an FDA-mandated study conducted by Xeljanz and Xeljanz XR’s manufacturer, Pfizer, found that patients taking the popular rheumatoid arthritis medication are at an increased risk of developing serious heart-related injuries.  Xeljanz is also used to treat psoriatic arthritis and ulcerative colitis. The preliminary results of the study were concerning…

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Why Was the Penumbra JET 7 Xtra Flex Catheter Recalled?

Wednesday January 6th, 2021 Defective Medical Devices, Firm News, Safety Information

On December 15, 2020, the U.S. Food and Drug Administration (FDA) announced Penumbra, Inc.’s recall of all Penumbra JET 7 Xtra Flex catheters due to the “risk of unexpected death or serious injury.” Penumbra, Inc.’s recall included a warning that all medical facilities who used the Penumbra JET 7 Xtra Flex catheter should remove them…

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Injuries Linked to the Penumbra JET 7 Xtra Flex Catheter Recall

Thursday December 24th, 2020 Defective Medical Devices, Firm News, Safety Information

Injuries Related to the Penumbra JET 7 Xtra Flex Catheter On December 15, 2020, the U.S. Food and Drug Administration (FDA) notified the public that Penumbra, Inc. had issued a voluntary recall of their Penumbra JET 7 Xtra Flex catheter due to reports of the product causing serious injuries and even death. The notice warned that…

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Penumbra Jet 7 Xtra Flex Catheter Recall

Tuesday December 15th, 2020 Defective Medical Devices, Defective Products, Firm News, Safety Information

The Food and Drug Administration (FDA) announced today that Penumbra has recalled all units of the Penumbra Reperfusion Catheter with Xtra Flex Technology (Jet 7 Xtra Flex) due to increased risk of serious injury and death while removing blood clots in stroke patients. Free Consultation The Penumbra Jet 7 catheter recall comes after the FDA received over 200…

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Symptoms of Hip Device Failure

Tuesday November 24th, 2020 Defective Medical Devices, Firm News, Safety Information

Hip replacements are among the most common orthopedic procedures in the United States. The operation is performed more than 300,000 times in the United States each year. During the procedure, a surgeon removes the damaged section of the hip joint and replaces it with artificial parts constructed of metal, ceramic, or hard plastic. Arthritis damage is…

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J&J Discontinues Sales of Talc-Based Baby Powder

Tuesday May 19th, 2020 Defective Medical Devices, Firm News, News, Safety Information

Johnson & Johnson announced today it was discontinuing sales of its talc-based baby powder products in the United States and Canada amid a firestorm of lawsuits claiming its signature product contains asbestos. The announcement comes just weeks after US District Judge Freda Wolfson ruled to allow testimony from plaintiffs’ experts in the New Jersey-based Multidistrict Litigation. Thousands of claimants…

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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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