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...
Feb 28, 2020 | Medical Malpractice, Uncategorized
Recalled Product MiniMed 600 Series Insulin Pumps Model 630G (MMT-1715) – all lots before October 2019 Model 670G (MMT-1780) – all lots before August 2019 Distribution Dates: Model 630G – September 2016 to October 2019 Model 670G – June 2017 to August 2019 Devices...
Apr 22, 2019 | Medical Malpractice, Uncategorized
This is a recall alert to all patients who received a Zimmer Persona implant prior to August 7, 2017. According to the recall filed with the FDA: “There is a potential for intermittent cracks in the raw material batch used to produce the affected products. The...
Mar 7, 2019 | Medical Device Failure, Medical Malpractice, Uncategorized
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product(s): CoaguChek XS PT Test Strips purchased from Terrific Care, LLC. or Medex Supply Lot Numbers: All lot numbers...
Jan 23, 2019 | Medical Device Failure, Medical Malpractice, Uncategorized
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Name: DORO® LUCENT Base Unit, Locking Transitional Member, and Transitional Member Serial numbers: 1704001,...
