StemCell Therapy

We Are Seeking Stem Cell Patients Who Have Experienced Complications or Adverse Medical Events

Injured by Stem Cell Products or Suffering from Complications? You May Be Entitled to Compensation.

The future of medicine is upon us stem cell therapy. Using stem cells to regenerate or replace damaged tissue or diseased cells is a technique that is offering new life to millions of patients.

Like any other medical treatment, stem cell treatments come with a number of risks and side effects, including stem cell rejection, Graft-versus-host disease (GVHD), fatigue, bruising or other minor side effects associated with stem cell procedures.

But some stem cell products carry greater, life-threatening risks.

Most Americans feel that stem cells are safe as long as they are FDA-approved or authorized for use in clinical trials. And this absolutely should be the case.

However, stem cell companies feeling pressured to keep up with a highly competitive market may skimp on quality control and ignore safe manufacturing requirements. Corrupt stem cell companies and clinics may use unsafe manufacturing conditions to save on costs, resulting in dangerous stem cell contamination and deadly patient infections.

Stem cell manufacturers and distributors who produce dangerous, defective, or contaminated stem cell products face criminal and civil penalties. Harmed stem cell patients have the right to file a lawsuit for damages, including past and future medical expenses, lost wages, pain and suffering, and other damages.

In an effort to crack down on this dangerous practice, our stem cell litigation firm is currently seeking reports of stem cell complications and adverse reactions. Working alongside the FDA, Department of Justice (DOJ) and Department of Health and Human Services Office of the Inspector General (HHS-OIG), we are actively investigating cases of potentially dangerous stem cell products.

Stem cells are cells found naturally in the body. But they are different from the majority of our bodys cells in that stem cells come from our own embryonic development. They exist throughout our lives, acting as a preliminary supply of cells from which new cells are derived.

As our bodys cells are damaged or die, stem cells are triggered to become or help create new, healthy cells to replace them. Many types of tissues contain stem cells:

Stem cells vary depending on the tissue they are taken from. Some can become any type of cell in the body, while others can become only one type of cell. This variation is grouped into five categories:

Injecting stem cells, implanting stem cells or growing stem cells to make artificial tissues have proven effective against numerous diseases.

Doctors currently use umbilical cord cells and adult stem cells to treat diseases like leukemia, multiple myeloma, lymphoma, neuroblastoma, and sickle cell anemia. Researchers are currently testing stem cell therapies to treat other types of cancers, heart disease, spinal cord injuries, stroke, type I diabetes, Alzheimers disease, amyotrophic lateral sclerosis, Parkinsons disease, severe burns, and osteoarthritis.

Scientists are also working on developing tissue regeneration techniques to grow organs and tissue for transplant, making everything from skin grafts and new blood vessels to healthy brain cells, heart cells, and kidney cells.

Currently, the FDA has approved the following stem cell-based products for use in the United States. All come from cord blood and function to produce various blood cell types.

As part of the 21st Century Cures Act (Dec. 2016), the FDA gives several unapproved stem cell therapies Regenerative Medicine Advanced Therapy (RMAT) designation. RMAT designated products, though not FDA-approved, have some preliminary clinical evidence of effectiveness against serious or life-threatening diseases for which no alternative treatment is available.

In addition to FDA-approved and RMAT-designated stem cell products, stem cell companies across the globe are currently developing and testing stem cell therapies for use in humans. Some of the primary stem cell companies include:

Like any other medical treatment, stem cell therapy comes with a number of risks and side effects. There are indirect risks, associated with other associated procedures like radiation or chemotherapy. Then there are direct risks that come with receiving the cells themselves.

Direct risks associated with stem cell therapies are relatively minor and temporary, typically lasting until the treatment takes and the cells become established in the body. The main risk is developing GVHD, when the bodys immune system tries to reject the cells, attacking healthy cells in the process. Symptoms include rash, jaundice, fever, diarrhea, cramping and nausea.

Other side effects of stem cell therapies may include fatigue (from temporary anemia), bruising (from temporarily low platelet counts), infection (from a temporarily weakened immune system).

Doctors will evaluate a patient for any potential risks up front and plan to address these issues accordingly, delivering medications before, along with, or soon after the stem cells to alleviate any problems.

However, when stem cells are not prepared or marketed correctly, serious, and life-threatening illness can result. Poor stem cell manufacturing practices can easily lead to contaminated cells. If contaminated cells are injected, the patient may develop sepsis, leading to loss of limbs, organ failure or death.

If stem cells are marketed as one type of cell but actually contain a different type of cell, those injected stem cells may cause organ failure, develop into tumors, or simply wont work as marketed allowing the patient to progress in their illness.

Even if you receive your own stem cells (autologous stem cell therapy), you can still suffer from a laboratorys poor cell acquisition process and bad preparation techniques. Your own stem cells can still become contaminated with viruses or bacteria during improper handling, causing highly dangerous infections after injection.

As the FDA ramps up its fight against unsafe stem cell companies, more and more stem cell clinics and laboratories are being disciplined for dangerous stem cell manufacturing practices.

Some stem cell products have received FDA approval and are already on the market. Others have obtained FDA investigational new drug (IND) approval or RMAT designation. According to the National Institutes of Health (NIH), more than 1,000 clinical trials examining stem cell therapies are currently underway.

All manufacturers of FDA-regulated stem cell products must adhere to strict FDA safety guidelines regarding manufacturing practices to ensure safety, potency, and purity. When they dont, they face both criminal and civil penalties.

Injured patients have the right to file a stem cell lawsuit for financial compensation, including money to pay for past and future medical expenses, lost wages, pain and suffering, and other damages.

Since properly prepared stem cell therapies rarely cause serious complications, you may be eligible to file a stem cell lawsuit if you suffered serious injury due to a stem cell product.[See our contact information at the end of this post.]

To meet FDA current good manufacturing practices (cGMP) requirements, stem cell companies must maintain a sterile facility to prevent risk of contamination. Live stem cells must be irradiated to ensure no bacterial or viral contamination is present.

Stem cell companies must also only market their cells for uses approved by the FDA. Telling patients or doctors that a stem cell line FDA-approved for lymphoma treatment is also useful for Type I diabetes treatment is dangerous and illegal.

Many stem cell products are manufactured overseas, making efficient FDA regulation difficult. With an FDA staffing shortage, overseas stem cell companies arent worried about surprise inspections and have no reason to maintain a sterile facility or sufficient quality control testing.

Most stem cell companies know an FDA inspection is coming months in advance, giving them time to clean up equipment, falsify quality control data and hide violations.

Because of the significant threat to public health, the FDA, DOJ and HHS-OIG rely on patients, doctors, nurses, stem cell laboratory technicians and pharmaceutical sales representatives to report cases of adverse reactions to stem cell treatments, stem cell contaminations and poor manufacturing practices.

Our stem cell litigation firm is currently working with the federal government to uncover potentially dangerous stem cell products. We are interested in hearing from anyone who has experienced serious complications after stem cell therapy.

Working with our national network of dangerous drug lawyers, we can help you receive answers and compensation. Stem cell products may be the future of modern medicine. Unfortunately, there are far too many companies rushing into the field with untested or dangerous products and making wild claims of miracle cures.

Recently FDA Commissioner Scott Gottlieb M.D. said,

The potential health benefits of regenerative medicine have spurred major progress in stem-cell biology over the past several decades. But we continue to see bad actors exploit the scientific promise of this field to mislead vulnerable patients into believing theyre being given safe, effective treatments; when instead these stem cell producers are leveraging the fields hype to push unapproved, unproven, illegal, and potentially unsafe products. This is putting patients health at risk.

Until the industry and regulators can insure that all medical products are safe and used properly, we will continue to protect patients and step in when drug companies push dangerous products or make unsupported claims. If you are suffering from an adverse reaction from stem cell products, contact us right away.

We are also seeking anyone with information on FDA cGMP violations, even third-party agents, outsiders, and international parties.

Present or former stem cell laboratory technicians, quality assurance (QA) professionals, pharmaceutical representatives, stem cell company executives, other stem cell safety or quality control specialists, physicians and nurses may be eligible for significant whistleblower awards under federal and state False Claims Acts.

You need not be a U.S. citizen or even a resident to report your concerns and receive a cash award.

For more information, visit our Dangerous Drug and Defective Medical Products page. If you have information on potentially dangerous stem cell preparations or are ready to file a stem cell lawsuit, Contact Us by Email at

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