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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 have Type 1 diabetes may use the MiniMed insulin pump to deliver insulin for the management of their diabetes. The Model 630G insulin pump may be used by persons sixteen years of age and older. The Model 670G insulin pump may be used by persons seven years of age and older. Reason for Recall Medtronic ...

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 ML Firm is investigating this safety risk and urges anyone with these implants to schedule an appointment with their physician. If you have been diagnosed with Lymphoma, you should contact our firm to discuss your options. The ML Firm is one of the very few that has taken one of the largest medical device companies ...

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 instrument as a result of the raw material issue.” Although this recall is from 2017, should you have a problem with a Persona implant, please call us to discuss your issues.

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. If you’re looking for the best lawyer, Mr. Meyerson is your man! I highly recommend him and I”m so thankful I got such a great lawyer to represent my case! Penny S. Midland, Texas Extraordinario, lubricación perfecta y ya sea una cura completa de la Viagra Genérico y ha sido aprobado para uso público, su efectividad tampoco será la máxima. Quiso dejar claro que “digitalizar no ...

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 2018 Distribution Dates: December 27, 2017 to December 15, 2018 Devices Recalled in the U.S.: 759 boxes Device Use The CoaguChek XS PT Test Strips, manufactured by Roche Diagnostics, are used with the CoaguChek XS System to monitor patient response to warfarin (also known by the brand names Coumadin and Jantoven), a blood thinner prescribed ...

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 July 5, 2018 Devices recalled in the U.S: 73 Device Use The DORO Lucent Headrest System is used to support the head and neck during brain and spine surgeries when immobilization is required. The headrest system has several parts including the base unit, the locking transitional member, and transitional member. Reason for Recall Pro-Med Instruments ...

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 27, 2018 Devices Recalled in the U.S.: 36 Device Use Synaptive Medical’s BrightMatter Guide with SurfaceTrace Registration provides detailed three-dimensional (3D) images of a patient’s brain to help surgeons safely navigate surgical tools used during brain surgery. Reason for Recall Synaptive Medical has initiated this recall due to a software defect found in the BrightMatter ...

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 man! I highly recommend him and I”m so thankful I got such a great lawyer to represent my case! Penny Scott Midland, Texas

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 purportedly ate a button battery from a generic Apple TV remote control that was sold by the company’s Web site. Recent Houston federal court records show that Morgan Gartner filed a product liability lawsuit on June 29. According to the suit, the child, identified by her initials E.G., ingested the part last Apr. 17. It adds the battery “became lodged in her esophagus.” “The electric current from the battery combined ...