Blogs & News
Medtronic Recalls MiniMed Insulin Pumps for Incorrect Dosing
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...
Allergan Breast Implant Recall
On July 24, 2019, Allergan plc announced a voluntary worldwide recall of BIOCELL® textured breast implants and tissue expanders. The FDA has indicated that these implants can cause a rare form of cancer called Anaplastic Large Cell Lymphoma in...
Recall of Zimmer Implants
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...
Another Happy Client!
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...
Terrific Care and Medex Supply Recalls CoaguChek XS PT Test Strips Used to Monitor Blood Thinner Warfarin Due to Inaccurate Test Results
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...
Pro-Med Instruments Recalls the DORO LUCENT Headrest Due to Possible Malfunction and Failure
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...