Sep 6, 2023 | Uncategorized
Abbott is recalling the Amplatzer Steerable Delivery Sheath due to an increased risk for air emboli to be introduced into patients who have procedures with this device. Air embolism can lead to injuries such as sudden (acute) reduction in blood flow to the heart...
Jul 26, 2023 | Uncategorized
Abbott is recalling the Amplatzer Steerable Delivery Sheath due to an increased risk for air emboli to be introduced into patients who have procedures with this device. Air embolism can lead to injuries such as sudden (acute) reduction in blood flow to the heart...
Nov 3, 2022 | Uncategorized
Do Not Use Infant Head Shaping Pillows to Prevent or Treat Any Medical Condition- FDA Safety Communication Today, the U.S. Food and Drug Administration (FDA) is warning parents, caregivers, and health care providers not to use infant head shaping pillows intended to...
Sep 1, 2022 | Product Liability, Uncategorized
The U.S. Food and Drug Administration (FDA) continues to warn consumers about the potential risk of injury associated with the use of certain brands of ultraviolet (UV) wands. Do not use these UV wands because they may expose you or any nearby person to unsafe levels...
Aug 31, 2022 | Medical Malpractice, Product Liability, Uncategorized
Integra is recalling the CereLink ICP Monitor, Model #826820/826820P, after reports that the device may display incorrect values for a patient’s intracranial pressure and display out-of-range pressure readings. If the device is not working properly, the patient may...
Aug 25, 2022 | Medical Device Failure, Medical Malpractice, Product Liability, Uncategorized
Medtronic, Inc. is recalling HeartWare HVAD System batteries because the batteries may experience electrical faults that cause them to unexpectedly fail. When this occurs, batteries with an electrical fault may be unable to power the controller, unable to accept...
