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Concerns Rise Over Potential Glass Particulates in Hospira’s Injections October 3, 2023 – Recent events surrounding the recall of certain medical injections have sparked an increased focus on pharmaceutical product safety and quality. On October 2, 2023, Hospira, Inc., a subsidiary of pharmaceutical giant Pfizer, made a concerning announcement that’s been rippling across the […]
Hospira Sodium Bicarbonate & Lidocaine
October 3, 2023 – Recent events surrounding the recall of certain medical injections have sparked an increased focus on pharmaceutical product safety and quality. On October 2, 2023, Hospira, Inc., a subsidiary of pharmaceutical giant Pfizer, made a concerning announcement that’s been rippling across the healthcare industry. The company has initiated a voluntary nationwide recall for its 4.2% Sodium Bicarbonate Injection, USP, as well as its 1% and 2% Lidocaine HCl Injection, USP, following fears over the potential presence of glass particulates within these products.
The injections in question, especially when tainted with foreign substances, pose significant health risks. The entry of glass particulate matter into the bloodstream can lead to severe complications such as inflammation within the veins, granulomas, and even life-threatening blockages in blood vessels. The risk, however, is somewhat mitigated, as medical professionals are advised to visually inspect injections for contaminants prior to use. Fortunately, Hospira, Inc. has not recorded any adverse events tied to these lots as of now.
Sodium Bicarbonate Injections, essentially electrolyte replenishers, play a vital role in treating metabolic acidosis, a condition that can arise due to various reasons such as severe renal disease or uncontrolled diabetes. The Lidocaine Hydrochloride Injection, on the other hand, is an antiarrhythmic agent used primarily to manage acute ventricular arrhythmias, especially during critical situations like cardiac surgeries.
Pfizer, ever-committed to patient safety, has reached out to all relevant stakeholders, urging them to cease the use and distribution of the affected products. They have emphasized the importance of immediate quarantine and have established channels for the return of recalled products.
While there haven’t been any reported adverse events connected to this issue, it’s crucial for potential victims to be aware of their rights. In cases where pharmaceutical companies fail in their duty to ensure the safety and efficacy of their products, affected individuals might have the grounds to file a product liability lawsuit.
In such lawsuits, victims can seek damages that might include compensation for medical expenses incurred due to the defective product, lost wages, pain and suffering, and, in unfortunate circumstances where death has resulted, funeral expenses. The legal framework also considers potential long-term health implications that could arise from such exposures. Thus, even if the immediate effects aren’t severe, the long-term ramifications could further contribute to the damages sought.
For victims or their families considering legal action, it is of paramount importance to consult with legal experts familiar with product liability cases. Expert legal teams can guide affected individuals through the often-complex legal pathways, ensuring they are adequately represented and that their rights are fully upheld.
If you or someone you know may have been affected by this recall, it’s essential to seek prompt medical attention and legal advice. Parker Waichman LLP, a nationally recognized product liability law firm, is offering a free consultation for potential victims. With their expertise in product liability cases, they can provide invaluable insight and guidance during these challenging times. Reach out to them at 1-800-YOUR-LAWYER (1-800-968-7529) to ensure that your concerns are addressed promptly and professionally.