Do You Have bad Product Buying Experience? Do You Have bad Product Buying Experience? If a defective product injured you, you have the right to file a lawsuit. If a defective product injured you, you have the right to file a lawsuit. Free Consultation Δ Free ConsultationProducts LiabilityProducts liability cases can be complicated, which is why youshould consider discussing your …
Drunk driving is a CrimeDrunk driving is a CrimeThe most serious – and dangerous – offenses a person can commitThe most serious – and dangerous – offenses a person can commit Free Consultation Δ Free ConsultationDrunk DriversDrunk driving is one of the most serious – and dangerous – offenses a person can commit.Drunk driving is one of the most serious …
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 …
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 …
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 …
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 …
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 …
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 …
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