Meeting Public Comments

Subcommittee meeting and times are as follows:
A bill for an act relating to product liability actions, including defenses.
Subcommittee members: Thomson, C.-CH, Scheetz, Wills, J.
Date: Wednesday, January 17, 2024
Time: 8:00 AM - 8:30 AM
Location: RM 103, Sup. Ct. Chamber
Names and comments are public records. Remaining information is considered a confidential record.
Comments Submitted:

01-16-2024
Gabby Fistler []
Vote No! Informed Consent Consumers should have the right to know that a products liability is limited prior to sale or use, especially in the case of medical products. Will this information be properly disclosed allowing the patient or consumer to make an informed decision prior to using it? Informed Consent requires the benefits, RISKS, and alternatives be discussed. Whether the risks are a side effect or the risk that a product causes injury due to negligence but you cannot hold the company accountable for it. Limiting Rights What problem is this solving that we need to again limit the rights of consumers/patients to hold companies accountable? When a product severely harms someone a lawsuit is often the only way the public will learn that a product is unsafe. Allowing for this limited liability will only encourage more dangerous products to be put on the market without as much accountability. The FDA is notorious for having weak or lax conflict of interest rules. A 2000 investigation by the US House Government Reform Committee found an overwhelming majority of members and consultants have substantial ties to the pharmaceutical industry they are responsible for over denying or approving. The rules that do exist are weak and their enforcement has been lax. Many are given waivers to participate in committee proceedings despite their known conflicts. The FDA continues to have to pull products from the market that they once considered safe and suitable for public use. Things like Acutaine, OxyContin, Levaquin, Cipro, Mirena birth control, Enfamil & NEC baby formula, etc.
01-16-2024
Ella Hall []
Manufacturers of any product should always be liable for faulty products that cause harm. If manufacturers were held accountable for their products, they would likely make safer products. The FDA has approved many pharmaceutical drugs that were later found to cause serious adverse health consequences such as liver or heart issues, and even death. Just because the FDA approves a product does not mean it is actually safe. Here are a few examples: https://prescriptiondrugs.procon.org/fdaapprovedprescriptiondrugslaterpulledfromthemarket/Why are we not trying to protect our citizen consumers from harm? Manufacturers should be making safe products. If they did, we would not need to worry about protecting a manufacturer, as this bill proposes to do.
01-16-2024
Jasanna Czellar []
Vote against! Why on earth would we want less accountability for manufacturers of products that can be life saving Or life threatening? When the FDA already has a proven track record of not pulling dangerous products until plenty are injured, why would we want to give companies more immunity? Most companies only care about bottom dollar so the ability to sue for a damaging product is essential to holding them accountable to honest and above board actions.
01-16-2024
Jennifer Leonhard []
Vote no. The FDA has a long history of having to pull products from sale after approval for sale. Patients are entitled to Informed Choice, which becomes more difficult as the availability and time a Dr can spend with a patient becomes more limited. Time and again we see pharmaceuticals be pulled when long term usage shows further injury to patient that was not discovered in phase 3 trials. Our laws are to protect Iowans, not for manufacturers to be free from liability that only encourages shoddy oversight. This bill endangers the citizens of our state rather than protecting them. I oppose this bill.
01-16-2024
Coreena Kinney []
Vote no! Giving manufacturers immunity for the harm their products do is definitely not going to make a product safer. Having to pay for those harms motivates the companies to make changes and make the products safer. The FDA has approved plenty of products that were later recalled, usually after hundreds of people were hurt. FDA approval is no guarantee of a safe product.
01-17-2024
Miranda B []
Please Vote no. Consumers have the right to know that there are rules protecting them from companies' greed to cut corners that might produce a harmful product. Where is the company's incentive to provide a wholesome, nonharmful product if the liability is relaxed? It's important to fight for the rights of the consumers. The companies will step up to provide a safe, quality product or go out of business... thus the way of the free market.
01-17-2024
Liz L []
I'm opposed to this. Making it harder to hold those who harm Iowans accountable is a disservice to us. Hundreds of biologicals and drugs are recalled by the FDA annually. I think this is the info a previous commenter was aiming for but I couldn't get their link to work https://datadashboard.fda.gov/ora/cd/recalls.htm
01-17-2024
Sarah Graham []
Please vote no. Its is very concerning that this bill even exists and for the legislators that believe this should go through I would ask what problem is this solving? What benefit is there in limiting the rights of consumers? Why would a legislator limit the rights of a consumer in holding a business accountable.
01-17-2024
Ella Hall []
The FDA is supposed to protect public health by ensuring safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation. has become known for promoting faulty products to American consumers. Unfortunately, the FDA's "approvals" have put consumers at risk. Florida's Attorney General Joseph Ladapo is trying to stop the Covid injections in human beings and Texas is suing Pfizer. Covid vaccination injuries were spotlighted on Capitol Hill by a group of physicians that were shedding light on the adverse side effects of COVID19 vaccinations. Consumers that took Covid shots are at risk because of the presence of DNA fragments in the shots. Upon examination of some vials, it was found that DNA contamination exceeds the FDAs10ng/dose requirements. DNA integration may result in chromosomal instability and cancer. In addition, vials of Covid shots showed contamination with SV40 (a known cause of cancer that has been in polio vaccines before). SV40 is linked to mesotheliomas, lymphomas and cancers of the brain and bone.The FDA never did any DNA integration assessments on mRNA Covid shots.Please do not pass ANY bill giving protection to big corporations when their products harm Iowa's citizens, especially based upon the fraudulent FDA standards. We must make these manufacturers responsible for their products if ever we are to have safe products.