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05/22/2015 - Any woman who has suffered an injury or adverse event relating to an Essure sterilization device is urged to file an Adverse Event report with the FDA as soon as possible. The FDA appears to be undertaking a half-hearted investigation into the serious and substantial allegations presented by thousands of women affected by the product. On April 2, 2015, three administrators from the advocacy group Essure Problems and two doctors met with 30 members of the FDA.
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05/20/2015 - Takata Corporation, a major manufacturer of automotive airbags, has now agreed to recall nearly 34 million defective airbags, making this the largest recall in US history, noted the US Transportation Department. By agreeing to a consent order that increases the number of recalled air bags, Takata has reluctantly committed to cooperate with the government. Takata has previously resisted taking full responsibility for the air bag problems, incurring thousands of dollars daily in fines levied by the US government.
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05/18/2015 - The U.S. Food and Drug Administration issued warnings on Friday concerning a newer class of type 2 diabetes drugs sold by Eli Lilly, AstraZeneca and Johnson & Johnson. The drugs may cause dangerously high levels of blood acids, which could require hospitalization. The medications, canagliflozin (Invokana), canagliflozin and metformin (Invokamet), dapagliflozin (Farxiga), dapagliflozin and metformin extended-release (Xigduo XR), empagliflozin (Jardiance) and empagliflozin and linagliptin (Glyxambi) may lead to ketoacidosis, a serious condition where the body produces high levels of blood acids called ketones, requiring hospitalization.
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05/18/2015 - Competing medications, Xarelto and Pradaxa, are not only in competition regarding which drug will take the lion’s share of the anti-coagulant market, but also which product will be the subject of the most lawsuits filed as a result of consumers injured by the medications.
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05/13/2015 - The Mirena IUD is Bayer’s most popular birth control product and worldwide sales have increased 33 percent between 2010 and 2013. However, recent studies showing adverse effects of the popular IUD may affect sales and the number of current lawsuits pending in the US concerning injuries caused by the device. Studies show a variety of injuries and symptoms are now being associated with the IUDs and more clinical studies are needed to completely understand the potential for problems.
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05/13/2015 - Pharmaceutical and medical device companies have historically opposed rules by the Food and Drug Administration (FDA) regarding the off-label use of medication and medical devices. When the FDA approves a drug or device, the drug label gives information regarding the drug, including the approved doses and how the drug is to be administered to treat the prescribed condition for which it was approved. When the drug is used in a different way other than described in the label, it is said to be an “off-label” use.
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05/13/2015 - Takata Corporation, the Japanese auto-parts supplier embroiled in a U.S investigation regarding exploding air bags, has confirmed at least six deaths and over a hundred injuries in documents provided to the Senate Commerce Committee. Several of the injuries caused by the air bags are serious, including quadriplegia, blindness, a broken sternum and multiple fractures.
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05/11/2015 - The number of testosterone lawsuits alleging serious side effects, including heart attack and strokes, has increased to nearly 1,400 claims pending in the multidistrict litigation in Illinois, according to court documents. The MDL, In Re: Testosterone Replacement Therapy Products Liability Litigation, is pending before Judge Kennelly in the Northern District of Illinois. Plaintiffs in the lawsuits claim they suffered from various health problems including heart attacks and strokes as a direct result of taking the testosterone.
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05/08/2015 - The FDA is warning the public and 14 sports supplement companies that one of the ingredients found in the supplements contain DMBA, a drug from the 1940s that raises blood pressure. DMBA has never been formally tested in humans so it is unclear how safe or effective the product is. The FDA has deemed that the sports supplements are adulterated with a new dietary ingredient that has no history or evidence of its safety. The FDA has warned the manufacturers of such products of the violations.
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05/07/2015 - Johnson & Johnson's Ethicon Inc lost its chance at a new trial after a jury returned a $5.7 million verdict in favor of a California women who claimed she was injured by the Ethicon mesh product. The jury ordered Ethicon to pay $700,000 in compensatory damages and $5 million in punitive damages for the irresponsible and negligent conduct of Ethicon.
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05/05/2015 - Women from around the country who have been harmed by Bayer's Essure birth control/sterilization device rallied today in San Fransisco to raise awareness about the Essure procedure and injuries the device can cause. Essure is advertised as a form of nonsurgical tubal ligation, but it is in fact, a painful surgical procedure. The group made their voices heard in front of the annual ACOG (American Congress of Obstetrics and Gynecology) meeting held at the Moscone Center in San Fransisco.
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05/03/2015 - This week Boston Scientific announced it had settled the first portion of thousands of legal claims filed against it by women suffering injuries from its transvaginal mesh products. The affected women were implanted with vaginal mesh products manufactured by Boston Scientific to treat pelvic organ prolapse and stress urinary incontinence. Many women were forced to endure several painful surgeries to have the eroded mesh removed from their bodies. Boston Scientific indicated it expected to pay nearly $119 million to resolve 2,970 cases.
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04/27/2014 - Ford Motor Company announced last week that it will be recalling 390,000 vehicles due to defective door latches, the latest in a series of recalls for door latch issues. This latest recall comes after two minor injuries and one accident occurred due to the defective latches. Since 2014, Ford has recalled over 1.4 million vehicles for door latches problems.
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04/27/2015 - FDA records reveal there has been a fifth death associated with the highly controversial Essure birth control device. Despite the demands of thousand of women nationwide, Bayer refuses to acknowledge the significant harm and injuries this device is inflicting upon thousands of women.
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04/26/2015 - For thousands of women suffering serious injuries after being implanted with the Essure sterilization device, one of the most frustrating obstacles they face is the lack of support by their implanting physicians. Hundreds of women with debilitating symptoms feel ignored and diminished when their own doctors readily dismiss their complaints.
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04/24/2015 - As transvaginal mesh cases continue to be litigated across the country, some meaningful headway is being made towards a global settlement of thousands of mesh cases. Some manufacturers such as American Medical Systems are actively negotiating settlement agreements while other companies are being dragged rather unwillingly to the settlement table.
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04/22/2015 - The first cases involving GranFlo and NaturaLyte dialysis solutions are scheduled to start trial on January 11, 2016 and February 16, 2016. Dialysis patients who were killed or injured by dialysis treatments involving GranuFlo and NaturaLyte products will be trying their cases before U.S. District Judge Douglas P. Woodlock in the district of Massachusetts.
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04/20/2015 - Americans spend an astounding $33 billion a year on dietary weight loss supplements, which claim everything from improved cognitive functioning to weight loss to increased muscle mass. Unfortunately many of these products either don’t work or are not safe. Some contain stimulants that have never been tested in humans while others have been tested and are considered dangerous.
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04/20/2015 - Women who took Zofran during their first trimester of pregnancy and delivered babies born with cleft lip, cleft palate or heart defects may be eligible to file a claim against Zofran manufacturer, GlaxoSmithKline (GSK).
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04/16/2015 - Zimmer Inc. has issued a voluntary recall for thousands of its Persona Knee implants, prompting the Food and Drug Administration to issue a warning that the implants can loosen, resulting in potentially serious complications. Zimmer stresses that the recall is voluntary, despite the FDA issuing a notice for a Class II Recall for all lots and sizes of the Zimmer Persona Trabecular Metal Tibial Plate knee implant. There are more than 11,650 devices, which may be affected by the recall.
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04/14/2015 - AstraZeneca’s new diabetes drug, Onglyza may be linked to an increased death rate according to preliminary studies reviewed by the Food and Drug Administration. The FDA has been extremely cautious regarding heart risks of diabetes medications following the catastrophic results of Avandia. An FDA advisory panel will meet today to discuss the safety of Onglyza and a similar drug called Nesina, manufactured by Takeda Pharmaceutical Co., the same company who developed Actos. The advisory panel was formed to review a trial of more than 16,000 patients who were taking Onglyza and had an increased risk of hospitalization due to heart failure.
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04/14/2015 - The country’s first Zoloft trial commenced last Thursday in St. Louis claiming that the popular antidepressant taken by women during pregnancy can cause serious and permanent birth defects. In this first trial, Plaintiff Kristyn Pesante claims her Zoloft use during pregnancy caused her son, Logyn Pesante to be born with multiple heart defects. Logyn was born with a transposition of the great arteries, known as TGA, in which the two main arteries of the heart are in the wrong place. He has suffered through six operations, over 25 procedures and lives with a pacemaker due to his condition. There are similar suits across the country in both state and federal court pending against Pfizer, the manufacturer of Zoloft.
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04/13/2015 - Potential claimants contemplating litigation often ask whether the litigation is a class-action lawsuit or a multidistrict litigation (MDL) and what the differences are between the two.
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04/09/2015 - A recent article authored by Dr. John R. Fischer for the American College of Obstetricians and Gynecologists shed some light on the problems women implanted with vaginal mesh continue to experience even after removal surgery attempts. The article, entitled, “What is New in the Use of Mesh in Vaginal Surgery” looked at data published in the last year on vaginal mesh. One of the most important points discussed in the article is that removing the problematic vaginal mesh does not always cure the problem.
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04/08/2015 - DePuy Orthopaedics announced it is accepting claims from ASR hip implant recipients who underwent revision surgery between August 31, 2013 and January 30, 2015 for defective ASR hip implants. However, the deadline to submit these claims is May 1, 2015. This second round of settlements offers similar benefits to the first program. Each individual claimant who meets the criteria begins with a base award of $250,000.
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04/07/2015 - In approving a new medication, the FDA must rely on numerous clinical studies to obtain information regarding the drug’s safety and efficacy. Most consumers are unaware that the FDA consistently reviews hundreds of clinical sites, which perform such clinical studies. However, according to a recent study released in JAMA Internal Medicine, there may be a number of errors or “departures from good clinical practice” in these studies.
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04/06/2015 - Patients who received a recalled ABGII Modular Hip System or a Rejuvenate Modular Hip System and underwent revision surgery prior to November 3, 2014 still have until April 17, 2015 to enroll in the current settlement program. On November 3, 2014, Stryker announced a $1.45 billion settlement to compensate patients who received a recalled hip device. Patients who had one hip implanted and removed prior to November 3, 2014 are eligible for $300,000 and patients who underwent a double hip replacement and revision can receive $600,000.
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04/06/2015 - Over 8,000 men and women across the country have decided to hold Takeda Pharmaceutical responsible for their contracting bladder cancer after taking the diabetes medication Actos. Recent verdicts across the country show that juries agree with the claimants and are taking the claims quite seriously.
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Thank you for visiting Ennislaw.com. Ennis & Ennis, P.A. is a plaintiff's national personal injury law firm concentrating on representing individuals who have been injured due to medication side effects, defective medical devices and defective products. Finding a qualified lawyer can be emotionally stressful and confusing. When you explore EnnisLaw.com we will empower you with our knowledge and experience. Not only can we guide you through every step of the legal process but we can also get you the compensation you deserve. Enjoy your visit to EnnisLaw.com. We update this site daily with news and developments on recalled drugs, devices and products. Join us on Facebook and share our site with your friends. We welcome your comments on our blog. Remember a consultation is free and confidential. Just call 1.800.856.6405 or fill out an online form.

Defective Drugs, Medical Devices & Products

Actos Bladder Cancer Lawsuit Lawyer
Actos side effects may include Actos Bladder Cancer. New study information has linked long-term Actos use with Bladder Cancer.

Accutane Inflammatory Bowel Disease | Crohn's Disease | Ulcerative Colitis
Accutane and it's generic versions (Amnesteem, Claravis, Isotretinoin, Roaccutane and Sotret) have been known to cause severe side effects such as liver failure, kidney failure, inflammatory bowel disease and ulcerative colitis.
Avandia Congestive Heart Failure | Heart Attack | Stroke  
Avandia side effects may include: congestive heart failure (CHF), heart attack and stroke. If you or a love done have been injured as a result of Avandia side effects you may be entitled to compensation.
Depuy Hip Implant Recall  
DePuy Pinnacle Ultamet Hip Implants are similar to the DePuy ASR because both are metal-on-metal implants. There have been a large number of complaints about the DePuy Pinnacle Hip Implant including: hip pain, loosening, metal fragments and a need for additional revision surgery.
Depuy Pinnacle Hip Replacement Lawsuit | Lawyer | Attorney  
DePuy ASR Hip Implants have been withdrawn from the U.S. market due to numerous reports of high failure rates in some patients which may lead to other injuries, excessive pain and the need for additional replacement surgery.
   
Smith & Nephew R3 Recall Lawsuit Attorney Smith & Nephew R3 Acetabular Hip Implant Liners have been recalled due to poor performance and reports of complications .
   
Defective Hip Implant Lawyer The Stryker Rejuvenate Modular Hip Implant, ABG II Modular Neck Stem Hip Implant & Stryker Accolade Hip Implant have been recalled due to fretting and corrosion at the modular neck junction which may cause early failure, metallosis, and need for revision surgery.
   
Biomet Metal on Metal Hip Implant Lawsuit Lawyer Biomet M2A Magnum Metal on Metal Hip Implant Lawsuit: The Biomet Magnum Hip Implant has had reports of high failure rates causing the need for revision surgery as well as other complications such as metallosis.
   
Stryker Knee Implant Recall Lawsuit

Stryker EIUS Unicompartmental Knee Implant System Recall Lawsuit: The Stryker EIUS Knee implant has been recalled due to a high failure rate and the need for revision surgery.

   
Transvaginal Mesh Implant Lawsuit
The FDA has recently warned about Transvaginal Mesh Implant complications and side effects. If you have been injured you may be entitled to compensation.
Fosamax Low Energy Femur Fractures Attorney  
Fosamax is a Bisphosphonate which is used in the treatment of Osteoporosis. Cases of Osteonecrosis of the Jaw and Low Energy Femur Fractures have been reported with Fosamax use.
   
Wright Medical Conserve Plus Cup Lawsuit

Wright Medical Conserve Plus & Profemur Hip Implants have had numerous reports of high failure rates in some patients. This may lead to other injuries, excessive pain and the need for revision surgery.

Meningits Lawsuit-Meningitis Lawyer-Methylprednisolone Acetate Recall Attorney

Methylprednisolone Acetate Meningitis Recall Lawsuit:
Tainted vials of methylprednisolone acetate have been recalled due to several reports of meningitis and deaths following injections of the contaminated steroid

Bard IVC Filter Recall Lawsuit Attorney

Bard IVC Filters - Bard G2 IVC Filter Recall Lawsuit::
Bard IVC Filters have been recalled due to reports of failure and/or breakage causing serious injury or death.

Paxil Birth Defects Lawsuit  
Woman who get pregnant while using the popular SSRI drug Paxil may experience Paxil Birth Defects particularly heart related birth defects as a result of Paxil use during pregnancy.
 
Plavix Side Effects Lawyer
Plavix side effects may include heart attack, stroke, cardiovascular disease and even death. Plavix has also been indicated to increase the risk of developing Intra cranial bleeding, gastrointestinal bleeding, lycophytic colitis and ulcerative colitis..
RV Refrigerator Fire
Dometic / Norcold RV Refrigerator Fire Recall:
Norcold and Dometic have recalled several models of RV refrigerators due to risk of fire that can result in serious injury or death to consumers.
Yaz Side Effects Lawsuigt  
Yaz, Yasmin, and Ocella are a type of birth control that have been linked to serious side effects such as heart attack, blood clots, stroke, and death in addition to other Yaz side effects.
Zimmer Hip Replacement Attorney  
Sales of defective Zimmer Durom Cup Hip Replacements have been suspended due to complaints of failure and crippling pain. Revision surgery may be needed in some patients to correct the problem.
   
Zimmer NexGen Knee Implants may fail early due to a design flaw which may cause it to loosen, cause pain and may require revision surgery.
Defective Zimmer NexGen Knee Implant Recall Lawsuit | Lawyer | Attorney
Zoloft Birth Defects  
Zoloft birth defects may include: congenital heart defects, persistent pulmonary hypertension, abdominal defects and cranial defects.
Prozac Side Effects Lawyer | Birth Defects Attorney  
Prozac birth defects have been reported when Prozac has been used during pregnancy.
Effexor Birth Defects | Antidepressant Pregnancy Risks | Effexor Lawyer  
Effexor Birth Defects have been reported when Effexor is used before conception or during the first trimester of pregnancy.
Bard Avaulta Transvaginal Mesh Support System Implant Recall Lawsuit  
Transvaginal Mesh Implant Lawsuit. The Bard Avaulta Plus Biosynthetic Support System has been recalled due to side effects resulting from the implant.
Vaginal Mesh Lawsuit Lawyer  
The Gynecare Prolift Pelvic Floor System, like many other popular brands of vaginal mesh, has recently been linked to several complications.
Ford Fire Recall Lawsuit | Attorney | Lawyer  
Ford Motor Company has recalled millions of Ford, Lincoln and Mercury vehicles due to a faulty cruise control switch that may cause the vehicles to burst into flames. Click here for more information about the Ford Fire Recalls.
   
Jeep Fire Gas Tank
Jeep Rear End Collision - Plastic Gas Tank Fire Lawsuit:: Jeep Cherokee, Grand Cherokee, and Liberty SUV fire lawsuit.
   
Vehicle Submergion Lawsuit - Auto Accident Lawyer  
Car accident lawsuit - vehicle submersion injury lawsuit. You may be entitled to legal compensation if you were involved in a vehicle submersion accident.
   
Propecia Sexual Dysfunction Lawsuit Propecia Sexual Dysfunction Lawsuit. Propecia (Finasteride) have been linked to erectile dysfunction that may be permanent.
CooperVision Avaira Contact Lenses Recall Lawsuit  
CooperVision’s AVAIRA Toric Soft Contact Lenses Recall issued due to an unintended presence of silicone oil residue, which can cause hazy or blurry vision, discomfort to the eye and injuries requiring medical treatment.
Medtronic InFuse Bone Graft Complications  
The Medtronic Infuse Bone Graft has been linked to serious and potentially life threatening complications when used in surgeries of the cervical spine, around the neck.
Covidien Duet TRS Recall Lawsuit Attorney - Tissue Reinforcement Staple Gun  
Covidien Duet TRS Recall. There have been reports of 3 deaths and 13 serious injuries associated with the use of the Duet TRS Tissue Reinforcing Staple Guns in the thoracic cavity (chest cavity).
   
Pradaxa Side Effects Pradaxa Side Effects Lawsuit:: Pradaxa side effects may range from problems with ulcers to internal bleeding and even death.
   
Mirena Side Effects Lawsuit
 
Mirena Side Effects Lawsuit. Mirena side effects may cause Ectopic Pregnancy, Uterine and Cervical perforation or the Mirena IUD could become imbedded in the uterus.
   
DMAA Side Effects Lawyer

DMAA side effects lawsuit. Products containing Dimethylamylamine or DMAA may cause serious side effects including heart attack, stroke, liver damage, kidney damage or sudden cardiac death.

   
Tekturna Side Effects Lawsuit

Tekturna Side Effects Lawsuit::
Tekturna (Aliskiren) , also marketed as Rasilez, has been linked to serious side effects such as kidney problems, stroke, and heart failure among other serious side effects.

   
Zithromax Lawyer - Z Pack Lawsuit Zithromax Side Effects Lawsuit:
Azithromycin, aka Zithromax, Zmax and Z-Pak has been linked to serious side effects such as liver damage, cardiovascular events like abnormal heart rhythm and sudden death.
   
Fresenius-Medical-GranuFlo-&-NaturaLyte-Dialysis-injury-lawyer Fresenius Medical GranuFlo & NaturaLyte Dialysis Injury Lawsuit: GranuFlo & NaturaLyte Dialysate Concentrates may raise bicarbonate levels in patients and cause sudden heart attack or other serious cardiac events or death.
   
Revatio Side Effects Lawsuit | Revatio Pediatric Pulmonary Hypertension Revatio Side Effects Lawsuit. Revatio use in children with pulmonary hypertension may cause serious and life threatening side effects such as heart failure or death.
 
Brilliant Blue G Recall Lawsuit Attorney Brilliant Blue G Recall - Lawsuit: Lots of Brilliant Blue G have been recalled due to suspected fungal contamination. The FDA has reported several cases of Brilliant Blue G induced eye injury such as fungal endophthalmitis.
   
Xarelto side effects may be serious and life threatening. Xarelto bleeding has occurred in some patients and has been fatal in some cases.
   
OMONTYS Side Effects Lawsuit Attorney Takeda & Affymax have issued a voluntary OMONTYS recall due to serious OMONTYS side effects including OMONTYS death from anaphylaxis.
   
Due to the potential for severe DePuy LPS Diaphyseal Sleeve side effects the FDA has announced a class I LPS Diaphyseal Sleeve recall. The device has the potential to fracture under normal load.
   
Lipitor side effects lawsuit - Lipitor side effects may include diabetes, kidney failure, liver failure, memory loss & rhabdomyolysis.
 
   
Tylenol Liver Failure Lawsuit Tylenol Liver Failure Lawsuit - Tylenol has been linked to severe side effects including liver damage and Acute Liver Failure (ALF).
   

If you or a loved one have experienced medication side effects or an injury from a defective medical device or product, you may be entitled to compensation. Call the lawyers of Ennis & Ennis, P.A. or fill out the form on this page for a free legal consultation.

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