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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The Center for Environmental Health (CEH) has filed a petition to the California Department of Toxic substances requesting that the state’s Safer Consumer Products program begin to regulate Bisfenol A (BPA) in canned food and beverages.
BPA is a chemical produced in large quantities for use in the production of polycarbonate plastics and epoxy resins.
Polycarbonate plastics are used in food and drink packaging, including water and infant bottles, safety equipment, and medical devices.
Epoxy resins are commonly found in lacquers that coat metal products such as food cans, bottle tops, and certain dental sealants and composites.
BPA is linked to many serious conditions, including:
Several countries like Canada and all of the European Union have banned PBA in some uses.
The U.S. has not banned its use and, in fact, the FDA continues to note that BPA is safe in its current approved uses in food containers and packaging.
Last year, California added BPA to its Proposition 65 list of chemicals known to cause birth defects, and then notified companies that they needed to begin warning consumers about their products containing the compound in May 2016.
But weeks before the deadline, an emergency rule was released without notice that allowed canned food companies to continue using BPA in their products without issuing warning to consumers.
Last month, the state also proposed extending the emergency rule to allow companies to avoid warning consumers at least through December 2017.
In response to the concern over BPA, the National Institutes of Health gave the following advice:
The NIH also recommends choosing glass, porcelain, or stainless steel containers over plastic ones, particularly for hot food or liquids.
Experienced Attorney & Legal SaaS CEO
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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Camp Lejeune’s water contamination issue spanned several decades starting in the 1950s. Exposure to these chemicals has been linked to various serious health issues, including cancer, organ diseases, and death.
Research is increasingly suggesting a link between the use of Tylenol during pregnancy and the development of neurodevelopmental disorders, such as autism and ADHD, in infants.
Legal action is being taken against manufacturers of Aqueous Film-Forming Foam (AFFF), a chemical used in fighting fires. The plaintiffs allege that exposure to the foam caused health issues such as cancer, organ damage, and birth and fertility issues.
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?
On Thursday, the FDA notified the public of a recall initiated by Abbott Diabetes Care Inc. of three lots of its FreeStyle Libre 3 sensor, which is a component of the company’s FreeStyle Libre 3 Continuous Glucose Monitoring System. The company says that the implicated
According to the FDA, Carson City-based company Sierra Stain LLC recalled three shades of water-based tattoo inks from its Bloodline brand due to the presence of high levels of microorganisms. Sierra Stain announced the recall on August 23, 2024. The recall pertains to three shades
The FDA recently notified the public of a recall issued by Inari Medical regarding updating instructions for use of its ClotTriever XL Catheter 30mm device after reports of injury and death. The recall does not involve the removal or discontinuation of the product itself, but