Attorney Jessie Paluch, founder of TruLaw, has over 25 years of experience as a personal injury and mass tort attorney, and previously worked as an international tax attorney at Deloitte. Jessie collaborates with attorneys nationwide — enabling her to share reliable, up-to-date legal information with our readers.
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While nearly 400 inferior vena cava (IVC) filter lawsuits are currently pending in the U.S., two class action IVC filter lawsuits have now been filed in Canada as well.
Cook Medical and C.R. Bard, Inc., the manufacturers of the largest share of IVC filters, face allegations that their devices were improperly designed and put patients at risk of serious injury.
As of March 23, 2016, there were 315 lawsuits consolidated for pretrial proceedings against Cook Medical in MDL 2570, and another 93 lawsuits consolidated against Bard in MDL 2641.
The plaintiffs in the Canadian IVC Filter lawsuits allege that their IVC filters broke apart and became lodged inside their bodies.
One of the patients claims that the IVC filter implanted in her body broke apart and one leg pierced her internal jugular vein and the rest migrating into her small intestines.
The woman’s doctors have told her that it is too dangerous to try to remove the device and consequently, she will have to take blood thinners for the rest of her life.
She and her husband filed a $200 million class-action lawsuit against Cook Medical in January 2016, alleging that she was never made aware of the potential risks involved with IVC filters.
IVC filters are implanted in the inferior vena cava to trap blood clots in patients who are at risk of pulmonary embolism but cannot take anticoagulant medications.
Retrievable IVC filters are meant to be temporary, used only until the risk of pulmonary embolism is gone and then removed, but many retrievable IVC filters are left implanted indefinitely, putting patients at an increased risk of device failure.
That risk prompted the FDA to issue a safety alert in 2010, warning that the retrievable IVC filters should be removed as soon as the patient no longer requires intervention to prevent blood clots.
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With over 25 years of legal experience, Jessie is an Illinois lawyer, a CPA, and a mother of three. She spent the first decade of her career working as an international tax attorney at Deloitte.
In 2009, Jessie co-founded her own law firm with her husband – which has scaled to over 30 employees since its conception.
In 2016, Jessie founded TruLaw, which allows her to collaborate with attorneys and legal experts across the United States on a daily basis. This hypervaluable network of experts is what enables her to share reliable legal information with her readers!
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AFFF Lawsuit claims are being filed against manufacturers of aqueous film-forming foam (AFFF), commonly used in firefighting.
Claims allege that companies such as 3M, DuPont, and Tyco Fire Products failed to adequately warn users about the potential dangers of AFFF exposure — including increased risks of various cancers and diseases.
Suboxone Tooth Decay Lawsuit claims are being filed against Indivior, the manufacturer of Suboxone, a medication used to treat opioid addiction.
Claims allege that Indivior failed to adequately warn users about the potential dangers of severe tooth decay and dental injuries associated with Suboxone’s sublingual film version.
Social Media Harm Lawsuits are being filed against social media companies for allegedly causing mental health issues in children and teens.
Claims allege that companies like Meta, Google, ByteDance, and Snap designed addictive platforms that led to anxiety, depression, and other mental health issues without adequately warning users or parents.
Transvaginal Mesh Lawsuits are being filed against manufacturers of transvaginal mesh products used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI).
Claims allege that companies like Ethicon, C.R. Bard, and Boston Scientific failed to adequately warn about potential dangers — including erosion, pain, and infection.
Bair Hugger Warming Blanket Lawsuits involve claims against 3M — alleging their surgical warming blankets caused severe infections and complications (particularly in hip and knee replacement surgeries).
Plaintiffs claim 3M failed to warn about potential risks — despite knowing about increased risk of deep joint infections since 2011.
Baby Formula NEC Lawsuit claims are being filed against manufacturers of cow’s milk-based baby formula products.
Claims allege that companies like Abbott Laboratories (Similac) and Mead Johnson & Company (Enfamil) failed to warn about the increased risk of necrotizing enterocolitis (NEC) in premature infants.
Here, at TruLaw, we’re committed to helping victims get the justice they deserve.
Alongside our partner law firms, we have successfully collected over $3 Billion in verdicts and settlements on behalf of injured individuals.
Would you like our help?
The California company C&A Naturistics is recalling its AK Forte supplement in response to a recent analysis that found undisclosed drugs in the product. According to the FDA, the company announced the recall last Thursday. The recalled product was sold online via Ebay and Etsy
The FDA warned consumers and health care providers today regarding a serious recall initiated by Staska Pharmaceuticals, Inc. of one lot of their Ascorbic Acid Solution for Injection (Preservative Free, Non-Corn) 500mg/mL, 50mL vials. The company issued the recall last Thursday after discovering potential contamination
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