Articles Posted in Drug Recalls

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The medical device injury attorneys at the Drug Law Center are now accepting cases involving defective innovative tissue regrowth stimulant silk netting products that cause injury.

What is Seri Surgical Scaffold Mesh?

Seri Surgical Scaffold Mesh RecallsIn recent years, Seri Surgical Scaffold Mesh devices have become highly popular among surgeons performing breast reconstruction and contouring plastic surgery procedures. The innovative silk netting material is designed to stimulate the regenerating growth of missing tissue. Doctors implant the surgical scaffold mesh device as a base for the regenerating tissue to provide strength to skin that has weakened and stretched.

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The chemical exposure injury attorneys at the Drug Law Center are currently accepting cases related to Roundup, Non-Hodgkin’s lymphoma and other diseases caused by carcinogenic chemicals in weed killing products.

What is Roundup?

Roundup RecallsRoundup is the most widely used weed killing product in the U.S. The broad-spectrum herbicide is chemically formulated to kill unwanted plants that threaten the growth of healthy crops. The weed killer contains the dangerous chemical glyphosate to block access to an enzyme that plants need to live. The product’s label reveals that the product is formulated with 41 percent glyphosate and 59 percent other active and inert ingredients that the labeling fails to identify.

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The supplement injury attorneys at the Drug Law Center are encouraging anyone who is been injured by a dangerous supplement to contact us today to discuss your legal options for compensation.

What is L-Citrulline?

L-Citrulline Drug RecallL-Citrulline is a non-essential amino acid that is converted into nitric oxide and L-arginine, and essential component to ensure health and vitality of the heart and blood vessels. Nitric oxide and L-arginine are known to boost the health of the body’s immune system.

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The IV flush syringe injury attorneys at the Drug Law Center are currently evaluating financial compensation cases involving injury caused by intravenous syringes.

What Is an IV Flush Syringe?

IV Flush Sirynge RecallsDoctors nurses and other healthcare providers use IV flush syringes to prevent blockages in IV catheters and remove any remaining drugs or left of her blood at a catheter site. Flushing syringes are also used after drugs have been delivered through the medicine for to ensure that the patient received the entire prescription. If the healthcare professional properly places the canoe look, the use of an IV flush syringe should be painless unless there is a discomforting interaction with the medication.

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The Infuse bone graft injury attorneys at the Drug Law Center fight aggressively for their clients who have suffered injury caused by the bone growth promoting device.

What Is Infuse Bone Graft?

Infuse Bone Graft RecallsSpinal surgeries to repair damaged or degenerating discs are common procedures in hospitals and medical centers throughout the United States. Nearly four-fifths of all spinal surgeries involved bone grafts. Originally, surgeons harvested the bone they needed from the patient’s own chin, hip, skull, or jaw bone. While the grafts were effective, the procedure created painful problems including secondary infections at the harvesting site. Nearly two decades ago, medical device manufacturers created synthetic versions of Infuse bone graft material that provided both positive results and horrific outcomes.

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The e-cigarette injury attorneys at the drug Law Center are now accepting cases on behalf of our clients who have suffered injuries caused by exploding e-cigarette devices.

What Is an E-Cigarette?

E-cigarette RecallsE-cigarette (also referred to as electronic cigarettes) vaporizes liquid nicotine and delivers the substance when inhaled by the user. The rechargeable handheld device contains a battery, atomizer, cartridge, and heating element. Many individuals enjoy the stimulation caused by the nicotine without inhaling the smoke of the traditional tobacco cigarette. However, these devices are not without their problems because they vaporize cancer-causing chemicals. Some have serious design flaws and have been known to explode without warning.

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The duodenoscope injury attorneys at the Drug Law Center are now reviewing information involving CRE infections that cause harm to patients following an endoscopic procedure.

What is the Duodenoscope?

Duodenoscope RecallsA duodenoscope is a lighted flexible tubing that doctors spread through the oral cavity, down the throat, and into the stomach to perform procedures on the duodenum (the top portion of the small intestine). More than 500 ERCP (endoscopic retrograde cholangiopancreatography) procedures are performed in America every year. The noninvasive procedures drained accumulating fluid from biliary and pancreas ducts that have been blocked by gallstones, tumors, or other serious condition.

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The Depo-Testosterone injury attorneys at the Drug Law Center are currently investigating cases for our clients who have suffered injury after taking the male hormone treatment medication.

What Is Depo-Testosterone?

Depo-Testosterone RecallsDepo-Testosterone is a treatment medication administered only through an intramuscular injection under doctor’s prescription. The drug contains androgenic hormone testosterone cypionate and is injected no more than one or two times every month. Doctors prescribe Depo-Testosterone for men who cannot make substantial levels of testosterone, the body’s natural male hormone. However, the medication is known to cause irreversible, dangerous side effects including shrunken testicles, enlarged breasts, high blood pressure, liver disease, infertility, heart attack, addiction, bone growth issues, stroke, and mental complications including increased levels of violence and aggression.

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The personal injury attorneys at the Drug Law Center are currently evaluating and accepting cases from clients who have been injured from a da Vinci robotic surgery procedure.

What Is da Vinci Robotic Surgery?

Da Vinci Robotic Surgery RecallsDa Vinci robotic surgeries are minimally invasive procedures controlled by a trained surgeon working through a console attached to a tower. The surgeon operates on the patient from a seated position using system controls while viewing the surgical site through a high definition 3-D magnified view on a stereoscope monitor. The system is built with four robotic arms where three arms hold and operate various surgical instruments and the fourth holds numerous 3-D cameras. The surgeon can also control the device using a foot switch.

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Contact the Biomet hip replacement injury attorneys at the Drug Law Center to discuss your rights to financial compensation if you have suffered serious injury by a defective medical device.

What is a Biomet Hip Replacement?

Biomet Hip Replacement RecallsZimmer-Biomet manufactures a variety of hip replacement devices to restore or replace a portion or all of a hip that is damaged by injury or in individual suffering from some condition like arthritis. Some of the products produced by the medical device manufacturer are used in hip resurfacing procedures or hip replacements surgeries that involve the acetabular liners and shells, and femoral heads and stems. Biomet first developed their M2a Magnum hip implant arthroplasty system in 2000.

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