Software Bugs Put Critical Care Patients at Risk
Increasingly, hospitals and other care providers are discovering that software errors are putting patients at risk.
For example, in February, the FDA recalled Smiths Medical’s Medfusion® 4000 Wireless Syringe Infusion Pump, which delivers a steady stream of medication to patients in critical care units, neonatal patients, and pediatric units. The devices that had older software configurations were found to disrupt patient care when bugs in the coding caused the system to shut off or deliver incorrect amounts of medication.
Technology Takes Hands-On Care From Patients
- Instead of administering medications to patients by hand, pumps wirelessly administer medications via intravenous infusion.
- Medical devices should receive greater attention when it comes to administering critical software updates, but often these updates are delayed or ignored.
- Outdated software puts patients at risk of receiving incorrect amounts of medication, either too much or too little.
- Properly trained nurses and attendees can be more reliable than technologies like these when they fail and malfunction. Backups should always be ready.
Contact an Experienced Product Liability Attorney
Thomas J. Henry are leaders in the area of product liability litigation. Our Defective Drug and Products Division has extensive knowledge and resources in order to represent our clients efficiently and aggressively. We represent a multitude of people who are battling against manufacturers of defective drugs and/or products.
Your choice does matter. If you or a loved one has suffered serious injuries because of a recalled product, call Thomas J. Henry immediately. We represent clients/victims all over the country. We are available 24/7, nights and weekends.