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,...
Jan 23, 2019 | Medical Device Failure, 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): Synaptive Medical, Inc. BrightMatter Guide with SurfaceTrace Registration Model/Product Numbers: SYN-0026...
Sep 7, 2018 | Medical Malpractice, Uncategorized
Five Stars! I am very pleased with Mr. Meyerson and his firm! They did a great job of getting me what I deserve! Mr. Meyerson and his colleagues took on a very tough case and won an unwinnable case. He and his staff are always so nice and understanding. I you’re...
Aug 9, 2018 | Medical Device Failure, Uncategorized
HOUSTON – A Texas woman is suing Amazon after her one-year-old daughter purportedly ate a button battery from a generic Apple TV remote control that was sold by the company’s Web site. HOUSTON – A Texas woman is suing Amazon after her one-year-old daughter...
Jun 18, 2018 | Medical Device Failure, Uncategorized
The ML Firm is currently representing patients who received the now recalled AccuLIF PL manufactured by Howmedica. This spinal fusion device incorporates a hydraulic component that increases its height after implant. Unfortunately, in certain patients, the device...
Mar 18, 2018 | Uncategorized
The ML Firm represents two families whose children recently swallowed button batteries. One is from an Apple TV knock off remote control purchased on Amazon, the other from a Polk Audio sound bar remote. Our firm is urging both companies to recall the products so that...
