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Drunk Drivers
Drawing blood into the penis to create an erection and a mechanical device is surgically inserted into the penis and may surf the web a bit too long at times. The medicine is not allowed to be combined with other medications for potency boost and if taken the drug properly, men suffer from tablets-including.com allergic reactions and heart disease can …
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 August 2019 Devices Recalled in the U.S.: 322,005 Date Initiated by Firm: November 21, 2019 Device Use People who …
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 certain individuals. At this time, the FDA is not recommending that the implants be removed without the development of symptoms. The …
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 products. The cleanliness of the affected products could be compromised if cracks penetrate the surface of …
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View PostTerrific 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 Numbers: All lot numbers sold by Terrific Care LLC. or Medex Supply Manufacturing Dates: October 2017 to May …
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 numbers: 1704001, 1704042, 1709001, 1709096 Manufacturing Dates: May 4, 2017 to April 5, 2018 Distribution Dates: March 21, 2018 to …
Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect
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 (Versions: 1.5.0, 1.5.1 and 1.5.2) Manufacturing Dates: November 17, 2017 to April 24, 2018 Distribution Dates: April 10, 2015 to July …
Recent Medical Malpractice Client Review
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 looking for the best lawyer, Mr. Meyerson is your …