Megadyne has recently received reports of 63 injuries (and counting) related to their MEGA 2000 and MEGA SOFT Reusable Patient Electrode devices.[1] The list of
The Actions against Bard seek to hold the device manufacturer liable for injuries caused by their wrongful conduct in connection with the design, development, manufacture,
Also commonly referred to as Injection Parts or Port-a-Catheters, the Bard PowerPort products at issue in these lawsuits are implantable vascular access devices designed to
Once you contact Rheingold Giuffra Ruffo & Plotkin LLP for guidance, you will be treated with the utmost professionalism, commitment, and respect. Our first meeting
In 2014, Covidien was acquired by Medtronic and now exists as one of Medtronic’s subsidiaries. Covidien hernia mesh products have been around for about two
There are dozens of models in the Covidien Symbotex line of hernia mesh implants that come in a variety of shapes and sizes. With so
The value of a Covidien hernia mesh lawsuit varies on a case-to-case basis and is determined by weighing a number of factors. These factors include,
On May 30, 2023, US Magistrate Judge Marcia M. Henry ordered that the discovery process be expedited in the Exactech mass tort litigation so that
Exactech is a multinational medical device manufacturer that designs and manufactures orthopedic medical devices such as joint implants. Recently in 2022, several thousand Exactech hip,
Q. What is a mass tort lawsuit? A. A mass tort lawsuit involves a product that causes injury to many people. Also known as a
The value of an Exactech recall lawsuit varies on a case-to-case basis and is determined by weighing a number of factors. Determinative factors include, but
By David B. Rheingold, Esq. STRATTICE™ biologic mesh is made with pig tissue as opposed to synthetic material. Litigations are located in New Jersey State
Hernia repair is a very common surgery with over one million operations performed annually in the United States.[i][ii] Surgeons have several options when it comes
Paragard, a type of intrauterine device (IUD) manufactured by Teva Pharmaceuticals, has been the subject of numerous lawsuits in recent years. These lawsuits have claimed that the
Last week the annual shareholder meeting of Johnson & Johnson took place at its headquarters in New Brunswick, New Jersey. Despite the proclamation of approvals
By Maria Markou, Esq. Honorable Judge Brian Martinotti supervises in a multi-county litigation (MCL) in Bergen County, where more than half of the nearly 1,500
By Paul D. Rheingold A respected securities analyst, Northland Securities, Inc. released a March 2013 advisory regarding Intuitive Surgical’s stock valuation. Due to the shortcomings
Many patients and physicians in New York are taking note of claims of injuries caused by robotic medical devices that are not being reported to
The Zimmer M/L Taper with Kinectiv Technology hip implant was voluntarily recalled in May, 2015. The FDA announced the Class I recall was issued because
Reuters (5/29, Dye) reports that Boston Scientific was ordered by a Delaware court on Thursday to pay $100 million to a woman who claimed injuries
A class I recall was issued in April, 2015, for all HeartWare Ventricular Assist Systems (VAS) currently in use. The HeartWare VAS helps deliver blood
By: Kelda Doherty It is no surprise to our firm that Johnson & Johnson, the largest manufacturer of health care products in the world, has
A California appeals court upheld an award of $3.61 million against C.R. Bard in a transvaginal mesh case. The Plaintiff received the Avaulta Plus transvaginal
A federal jury in West Virginia awarded four plaintiffs $14.5 million in compensatory damages and $4 million in punitive damages in a Boston Scientific TVM
Johnson & Johnson, the manufacturer of drugs and medical devices among other products, was ordered by a Jury in California to pay $5.7 million. The
A recent Wall Street Journal report found that 14 deaths were tied to Medtronic’s SynchroMed drug-infusion pumps. The Department of Justice (DOJ), in conjunction with
FDA announced a Class I Recall of the Tiger Paw System II, produced by Maquet Medical Systems. The Class I is the most serious FDA
The FDA has issued its most serious recall, Class 1, on MicroPort Orthopedics’ Profemur Long Cobalt Chrome 8 Degree Varus/Valgus Modular Neck devices. The Shanghai-based
By Maria Markou, Esq. On April 11, 2014, Judge Joseph R. Goodwin, who presides over six vaginal mesh multidistrict litigations in West Virginia, ordered the
by Maria Markou Our firm specializes in representing people with serious injuries as a result of harmful medical devices and drugs. Recent FDA recall statistics
by Maria Markou The Rheingold product liability trial litigation team has represented many injured clients and wrongful death cases against Johnson & Johnson: DePuy Pinnacle
By: Indhira Benitez As recently reported, Minnesota anesthesiologist, Dr. Scott Augustine, has been campaigning to remove the device he helped create off of the market.
By: Kelda Doherty The United States Judicial Panel on Multidistrict Litigation (JPML) has this month ordered that pre-trial proceedings concerning the Stryker’s Rejuvenate and ABG
