Manufacturer Medline Industries initiated a recall of its Hudson RCI Addipak Unit Dose Vial, 0.9% full normal saline solution in July of this year. The FDA has categorized this recall as a Class I recall, which is the most severe kind of recall, reserved for cases in which use of…
Bard’s PowerPort devices are implanted under the skin and pump intravenous chemotherapy and other fluid into a patient’s bloodstream. These are two-part devices with an injection reservoir and a catheter. Recently, plaintiffs in eight lawsuits against Becton, Dickinson & Company, C.R. Bard, Inc., and Bard Access Systems made a motion…
Earlier this month, the Food and Drug Administration (FDA) issued a warning regarding Photo Credit:g0d4ather/Shutterstock.com two breast implant manufacturers for their failure to comply with specific regulatory requirements. According to the official FDA press release, the FDA sent warning letters to Allergan and Ideal Implant Incorporated. The Warning Letters Under…
Medical products and devices are often used in surgical procedures and other medical treatments. In some cases, these devices can save lives. However, sometimes these devices can be dangerous and may result in more serious injuries than the injuries they are used to treat. Pelvic mesh, sometimes called vaginal mesh…
In a recent case, a woman had surgery done at a hospital and subsequently suffered a stroke. The woman filed a products liability claim against the manufacturer of one of the medical devices in the surgery. However, when the complaint was originally filed, it did not name the hospital or the doctor…
With advances in medical technology, many medical procedures that used to be daunting are now routine. Patients often arrive at a hospital or surgical center early in the morning and leave by mid-afternoon with few after-effects from the procedure or anesthesia. Many are able to even return to work the…
A Tennessee-based medical device company has issued a recall for a prosthetic part used in hip joint replacement surgeries. According to one news source, the recall is a Class I recall. Class I recalls are issued when there is a reasonable probability that continued use of the device will cause…
According to news reports, eight patients who underwent heart bypass surgery at a Pennsylvania hospital most likely suffered bacterial infections because of a contaminated medical device used during the surgeries. The device is a heater-cooler unit used to control a patient’s blood pressure during open-heart surgery. Of the eight patients…