When medical devices backfire, it can lead to much havoc on a patient’s health. Currently, the Bard PowerPort is facing a similar predicament. The device was designed to manage medications correctly and quickly through a catheter. However, several patients have reported issues such as catheter dislodgement and breakage of materials, leading to severe health risks.
Owing to these adverse effects, patients today are filing product liability claims against the manufacturer. In this article, we will discuss the hazardous side effects of Bard PowerPort, such as pulmonary embolism, and share how patients can opt for a legal remedy.
Functions and Flaws of Bard PowerPort
Just like any other medical device, the Bard PowerPort is made with metal or plastic and comprises a catheter and port design. The port is intended for power injection, which facilitates quick infusion of substances into the bloodstream.
Typically, the device is attached to a major vein, usually the chest. It indicates very little scope for error, and it can result in any injury during a malfunction. Yet, there have been several complaints concerning catheter tubing’s structural weaknesses. Also, all these problems can hurt the integrity of the tube, increase bacterial growth, and cause the device to break down or get displaced during treatment.
Some issues include an irregular heartbeat, blood clots, heart punctures, deep vein thrombosis, internal perforations, and hemorrhaging. There have been patients like Johanna Randow who, in their port catheter lawsuit, have reported suffering from pulmonary embolism as well.
The Tragic Story of Johanna Randow
Johanna Randow, a cancer patient from Maryland, had filed her product liability lawsuit at federal court in Arizona against C.R. Bard and Bard Access Systems. She is one of the many others who have filed a complaint against the company for the pain and adversity she underwent.
Under medical supervision, the Bard Infuse-A-Port device was implanted in her body as a part of her chemotherapy treatment. Almost a year later, this port had to be removed since it wasn’t functioning correctly. Two years after this incident, she developed a pulmonary embolism.
Johanna wondered what could have led to this. A medical assessment revealed that after the device got implanted, it got fractured, which sent fragments into her heart, thereby leading to pulmonary embolism.
Her lawsuit states that a few fragments of the catheter device might have stayed close to her heart, which has made her vulnerable to other injuries in the future. The possibility of this can add to stress and tension, which is not conducive to the treatment she is undergoing for her cancer.
Other Complications of Bard PowerPort Devices
Some severe complications that come with this catheter device include an abnormal heart rate and even organ damage. Once fragments of a fractured device get spread into the patient’s bloodstream, they can rupture blood vessels and puncture organs.
The complications are:
- Chest Pain
- Blood Cough
- Shortness of breath
- Urinary changes
When a catheter device becomes defective, it can accumulate bacteria and lead to infection that affects the health of a patient heavily. When it is left untreated, an infection can cause sepsis that affects the entire body.
Pinch-Off Syndrome: A Serious Bard PowerPort Complication
Pinch-off syndrome takes place when a catheter gets pinched between the patient’s rib and clavicle, thereby blocking the tubing. A few symptoms of pinch-off syndrome include challenges in passing fluids via the catheter and even drawing blood.
As and when a doctor or any medical provider suspects that a patient is suffering from this syndrome, they will inspect it on priority. They will conduct an X-ray to check whether the condition is severe and requires surgery to remove the device.
The Role of a Lawyer
Have you suffered from pulmonary embolism or any other complication due to Bard PowerPort implantation? If so, it is a wise decision to seek legal recourse to ensure that you get compensated for the damages you have endured.
According to TorHoerman Law, patients should contact a lawyer before going ahead with a claim with any medical device manufacturer. It is because such legal cases are challenging and might require patients to use accurate evidence to ensure they get the justice they want. Furthermore, the lawyer’s advice and guidance will ensure that they are covered for all economic and non-economic damages.
Finally, when medical device manufacturers become negligent about the product they are promoting, it can lead to severe complications among patients. The Bard PowerPort is being heavily complained about today because of device fracture and health complications it carries.
Whether they have suffered from pulmonary embolism or an abnormal heartbeat, patients need to preserve and present their medical documents while filing a legal complaint. Once it’s established that their health issues are a result of device malfunctioning, a lawyer can help in acquiring both justice and fair compensation.