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Ennis & Ennis, P.A. is a national mass tort law firm that specializes in handling individual cases for people that have been injured as the result of medication side effects, defective medical devices, and product liability. If you or a loved one have been injured, contact the lawyers of Ennis & Ennis, P.A. today for a free legal consultation.
 
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11/05/2009 - MARSHALL - A Marshall resident and an Arizona resident believe they are the victims of zinc poisoning and possible neurological damages caused by their ingestion of Super Poligrip Denture Adhesive Cream. More>>>

11/05/2009 - Three Illinois residents say they are susceptible to sudden shocks after defective implantable defibrillators manufactured by Medtronic were inserted into their hearts. Lillian Tengstrand, Effie Thomas and Marcus Williams filed a lawsuit Oct. 14 in St. Clair County Circuit Court against Medtronic, Medtronic USA, Medtronic International Technology and Medtronic Puerto Rico Operations. More>>>

11/05/2009 - Some treatment plans for type 2 diabetes may need to be modified, as the FDA has prompted prescribing information changes for the popular drug Byetta. According to the FDA, from April 2005 until October 2008, 78 reports of impaired kidney function was reported. More>>>

11/04/2009 - Refusing to accept the explanation of Toyota and the federal government, hundreds of Toyota owners are in rebellion after a series of accidents caused by what they call "runaway cars." Safety analysts found an estimated 2000 cases in which owners of Toyota cars including Camry, Prius and Lexus, reported that their cars surged without warning up to speeds of 100 miles per hour. More>>>

11/04/2009 - Results of a new study suggested that prescription of antipsychotic drugs for children could be a factor in their rapid weight gain and may raise the risk for diabetes and heart disease. More>>>

11/04/2009 - The U.S. Food and Drug Administration on Monday said it approved a new label for the diabetes treatment Byetta, made by Eli Lilly & Co. (LLY) and Amylin Pharmaceuticals Inc. (AMLN), amid reports the medicine may cause kidney problems. More>>>

11/03/2009 - Reports about possible kidney problems, including renal failure, in people taking the diabetes drug exenatide (Byetta) have prompted changes to the drug's prescribing information, the U.S. Food and Drug Administration said Monday. More>>>

11/03/2009 - Toyota said today that its cars don't have a rampant sudden acceleration problem for any reason other than driver’s side floor mats that can become lodged under the gas pedal. More>>>

11/03/2009 - Patients and doctors should be aware of possible kidney function problems with Eli Lilly and Amylin Pharmaceuticals' Byetta diabetes drug, U.S. health regulators said on Monday. The U.S. Food and Drug Administration received 78 reports of problems with kidney function in patients using Byetta from April 2005 through October 2008. More>>>

11/02/2009 - A U.S. safety board declined further investigation into an alleged defect that may cause uncontrolled acceleration in Toyota Motor Corp.’s Lexus ES sedans after the carmaker issued a recall this month for floor mats. More>>>

11/02/2009 - The U.S. Food and Drug Administration today acted on new safety information about possible kidney function problems, including kidney failure, in patients taking Byetta (exenatide), a drug used to treat Type 2 diabetes. From April 2005 through October 2008, the FDA received 78 reports of problems with kidney function in patients using Byetta. More>>>

11/02/2009 - So your doctor says it's time to consider that hip replacement. Trouble is, more than a dozen firms make artificial hips, and there've been plenty of recalls—no small inconvenience when the recalled product resides in your pelvis. More>>>

11/01/2009 - Parents say their daughter committed suicide because drug companies failed to warn them of the side effects of their acne drugs. Their daughter, whose age is not specified, killed herself after taking Claravis and YAZ for acne, the parents claim in Mahoning County Court. More>>>

11/01/2009 - Results from a retrospective study presented here at the American College of Gastroenterology (ACG) 74th Annual Scientific Meeting suggest that use of isotretinoin is associated with the development of inflammatory bowel disease (IBD). More>>>

11/01/2009 - Drugmaker AstraZeneca P.L.C. said yesterday that it had set aside $520 million as part of a tentative agreement to resolve an investigation by federal prosecutors in Philadelphia into the company's marketing practices. More>>>

11/01/2009 - It's been over a month since Madison County Circuit Judge David Hylla heard arguments in a case over the acne drug Accutane and, with the case's Oct. 19 trial date past, he is scheduled to hear more motions in the suit on Nov. 3. More>>>

11/01/2009 - Let’s look at the numbers behind AstraZeneca’s Seroquel settlement with the U.S. Disrict Attorney in Pennsylvania. The headline number is $520 million, the amount AstraZeneca (AZN) will pay to end a probe of its marketing practices on the atypical antipsychotic, which allegedly resulted in off-label use of the drug in children and the elderly. More>>>

10/29/2009 - A federal appeals court on Wednesday reinstated a shareholder lawsuit against Scottsdale-based Matrixx Initiatives over what company officials knew about potential dangers from its popular Zicam cold remedy. In a unanimous ruling, a three-judge panel of the 9th U.S. Circuit Court of Appeals said that U.S. District Court Judge Mary Murguia was wrong to throw the lawsuit, filed in 2004, out of court. More>>>

10/29/2009 - A growing association between a widely used multiple sclerosis drug Tysabri (natalizumab) and a potentially deadly brain infection has been reflected in strengthened warnings for prescribers and patients. More>>>

10/28/2009 - From Australia comes word that San Diego-based Amylin Pharmaceuticals’ biggest drug, exenatide (Byetta), has been caught up in a controversy over a diabetes report co-sponsored by Amylin’s marketing partner, Eli Lilly & Co. More>>>

10/28/2009 - A Minnesota state court judge has dismissed a batch of lawsuits against Medtronic Inc stemming from the October 2007 recall of the medical device maker's Sprint Fidelis defibrillator leads. More>>>

10/27/2009 - Ennis & Ennis, P.A. announces today it is still investigating and accepting Accutane cases against the manufacturer of the drug Hoffman La-Roche. David Ennis states, "although Hoffman La-Roche announced in June 2009 that it will no longer sell Accutane due to generic competition and large legal costs defending the drug this does not absolve La-Roche from liability from patients who took the drug in the past and have suffered Inflammatory Bowel Disease (IBD), Ulcerative Colitis and Crohn’s Disease". More>>>

10/27/2009 - Matrixx Initiatives Inc (MTXX.O) said the U.S. health regulator has indicated that it is unwilling to reverse its position regarding the warning letter issued on company's nasal versions of Zicam cold remedy. In June, the company voluntarily withdrew two of its existing Zicam products after the U.S. Food and Drug Administration issued a warning letter that the products could cause a loss of smell. More>>>

10/27/2009 - Bayer faces almost 1,000 lawsuits in a Florida federal district court regarding its anti-bleeding drug Trasylol, according to the docket in the case (1:08-md-01928-DMM). While there have been sporadic reports in local media of people filing claims against Bayer alleging Trasylol contributed to renal failure, there has been little overall publicity to what is clearly a massive multi-district litigation effort going on in Judge Donald Middlebrooks’ Southern District federal court. More>>>

10/27/2009 - A federal report on the fiery, high-speed Lexus crash that killed a California Highway Patrol officer and his family found that the accelerator was stuck to an unsecured and incorrect floor mat and that the design of the gas pedal may have contributed to the crash. More>>>

10/26/2009 - Federal highway safety inspectors have released new details of a fatal car crash that triggered Toyota Motor Corp.’s largest recall, including a finding that the Lexus ES 350 sedan involved had a gas pedal design that could increase the risk of it being obstructed by a floor mat. More>>>

 

News Archive ::

 
     
FDA News
 

11/04/2009 - Centurion Medical Products and FDA notified healthcare professionals about a Class I recall of Premie Pack, Kit Code LM 110 and Full Term Meconium Pack, Kit Code LM115. More>>>

 

 

 
     
FDA MedWatch
 

11/04/2009 - Bodybuilding.com and FDA notified healthcare professionals and patients of a nationwide and international recall of all lots and expiration dates of 65 dietary supplement products that were sold through the Company's website, www.bodybuilding.com. More>>>

11/02/2009 - FDA notified healthcare professionals of revisions to the prescribing information for Byetta (exenatide) to include information on post-marketing reports of altered kidney function, including acute renal failure and insufficiency. More>>>


MedWatch Archive ::


 
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Avandia Side Effects   Avandia side effects may include: congestive heart failure (CHF), heart attack and stroke. If you or a loved one have been injured as a result of Avandia side effects you may be entitled to compensation.
     
Accutane   Accutane has been known to cause severe side effects including liver failure, kidney failure, IBD, Crohn's disease and ulcerative colitis.
     
Animas Insulin Pump   Animas Insulin Pumps and the FDA has issued a recall of battery caps used with the OneTouch Ping System, Animas 2020 Insulin Pump, Animas IR1200 Insulin Pump, and Animas IR1250 Insulin Pump.
     
Actavis   Actavis Inc. voluntarily recalled 14 lots of Fentanyl transdermal system Cll patches that were sold in the U.S.
Actavis Recalls Remaining Fentanyl Patches in the US as Precaution
     
IAB Catheter Lawyer  

Arrow IAB Pump Catheters have been recalled because they may contain defective volume connectors for the 30cc, 40cc, and 50cc sizes. This can cause the pump to deliver the wrong dose of medication and result in serious injury.

     
Baxter Colleague Infusion Pump Lawsuit   Baxter Healthcare Corp. in association with the FDA has recently issued a Class 1, worldwide recall of the COLLEAGUE Volumetric Infusion Pumps due to safety issues.
     
Byetta Side Effects   Byetta (exenatide) is a type 2 diabetes drug used to help reduce blood sugar levels. Recently, Byetta has been linked to serious cases of pancreatitis and in some cases death.
     
Chantix Suicide Lawsuit   Chantix (varenicline) is a drug used to help patients quit smoking. According to the FDA, Chantix has been linked to serious side effects including suicide and suicidal thoughts.
     
Denture Cream Lawsuit   Denture Creams have recently been linked to serious side effects such as Zinc Poisoning, Neuropathy, and other neurological problems. Zinc Poisoning often is misdiagnosed as other demyelinating diseases.
     
Digitek (digoxin) Recall   Digitek (digoxin) is a drug used to treat heart failure and abnormal heart rhythms. A recent class I recall has been issued on all Digitek (digoxin) tablets, which may contain twice the approved level of digoxin.
     
Duragesic   The DURAGESIC (fentanyl transdermal system) CII patch is a strong medication for moderate-to-severe chronic pain. Patches can leak and cause injury.
Breaking News....More Duragesic Fentanyl Patches Recalled due to manufacturing defect that may result in overdose.
     
Ethex Recall Attorney   Ethex Drug Recall: Over the past year the Ethex Corporation has recalled several of its drugs due to a manufacturing defect causing the pills to be oversized. This can cause serious side effects, overdose, or death. *** BREAKING ETHEX RECALL NEWS ***
     
Evenflo High Chair Recall   Evenflo has recalled of about 643,000 Envision high chairs and expanded a recall of 90,000 Majestic model high chairs. Both models of high chairs were recalled due to risks from falls and choking hazards.
     
Fleet Phospho-Soda Kidney Damage Lawsuit   The use of oral sodium phosphate solutions like Fleet Phospho-soda have been linked to an increased risk of kidney injury, known as Acute Phosphate Nephropathy, which could lead to renal failure, the need for dialysis treatment, a kidney transplant or even death.
     
Fluoroquinolone Side Effects  

Fluoroquinolones are a type of antibiotic used to treat bacterial infections. They have been linked to serious side effects such as tendonitis, ruptured tendons, and torn ligaments.

     
Fosmax   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.
     
Gadolinium   Have you had an MRI? If so it may have been with done with a contrast agent that contained gadolinium. Click here for more information about Gadolinium MRI contrast agents.
     
Gardasil HPV Vaccine Side Effects   Gardasil is a vaccine developed by Merck & Co for certain strains of human papilloma virus (HPV). The vaccine has recently come under scrutiny as a result of studies linking it with a number of potentially fatal side effects.
     
Heartmate II Recall   On October 26, 2008 Thoratec Corp. issued a recall of its “HeartMate II LVAS” mechanical heart pumps after receiving reports that 5 people have died while using the device and at least 27 reports of need for replacement.
     
Heparin Sodium
  Heparin sodium is a blood thinner that is commonly administered into the vein of patients. Baxter Healthcare had a voluntary recall of several of its vials due to a potential contamination.
   
 

Hydroxycut Side Effects Recall Lawsuit:
Hydroxycut has been recalled due to serious side effects such as liver damage, liver failure, and death.

     
Infant Warmer Recall Lawyer   Stabilet Infant Warmer Recall Lawsuit:
A class 1 recall has been issued on certain models of Stabilet infant warmers due to fire risk that may result in serious injury or death of infant or caregiver.
     
Ketek   According to the FDA, Ketek may be responsible for serious side effects such as Liver Failure and Stevens Johnson Syndrome
   
Levaquin Side Effects Lawsuit-Fluoroquinolones   Levaquin is an antibiotic in the fluoroquinolone family. It has been linked to serious side effects such as tendonitis, ruptured tendons, and torn ligaments.
     
Maytag Refrigerator Fire Recall  

Maytag Refrigerator Fire Recall:
On March 10, 2009 the U.S. Consumer Product Safety Commission in conjunction with Maytag Incorporated issued a voluntary recall on 1.6 million refrigerators due to a fire hazard.
***BREAKING NEWS*** RECALL EXPANDED IN AUG. 2009

     
Dometic / Norcold RV Refrigerator Fire Recall Lawsuit   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.
     
Medtronic Infuse Bone Graft   The Medtronic Infuse Bone Graft has recently been linked to several cases of death or life-threatening complications when used in surgeries on the upper spine and neck.
     
Defective Medtronic Pacemakers - Pacemaker Wire Seperation - Kappa - Sigma   Medtronic recently sent out a "Dear Doctor" letter warning about defective Kappa and Sigma series pacemakers. Pacemaker wire seperation may lead to device failure causing serious side effects and even death.
     
Ortho Evra   The Ortho Evra Birth Control Patch has caused serious side effects for many women who have turned to the patch as an alternative to traditional birth control pills.
   
Peanut Butter Recall Lawyer   On January 10, 2009 the FDA in conjunction with King Nut Companies & Peanut Corporation of America (PCA) initiated a nationwide recall of peanut butter distributed under the King Nut label. due to an outbreak of salmonella food poisoning.
     
  Abbott POWERSAIL Catheter Recall:
On July 28, 2009 Abbott conducted a voluntary recall of three lots of POWERSAIL Coronary Dilatation Catheters from United States distribution and one lot from international distribution.
     
 

On February 26, 2009 the U.S. Food & Drug Administration (FDA) added a “Black Box Warning” to metoclopramide-containing drugs, including Reglan tablets, Reglan oral disintegrating tablets, metoclopramide oral solution, and Reglan injections due to the risk of Tardive Dyskinesia.

     
 

Raptiva has recently been linked to life threatening side effects such as progressive multifocal leukoencephalopathy (PML) and other serious infections.
***Breaking News: Raptiva Withdrawn From U.S. Market***

     
  Seroquel Side Effects Lawsuit:
Seroquel has been linked to serious side effects such as diabetes, pancreatitis, and tardive dyskinesia.
     
Dilantin Lawsuit   The FDA has recently issued an alert for Phenytoin & Fosphenytoin regarding a potential increased risk of serious skin reactions including Stevens Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN)
     
  Spiriva Handihaler has been shown in recent studies to increase the risk of heart attack, stroke, and cardiovascular death.
     
Stryker Cranial Implant Recall   Stryker Leibinger USA and the FDA have issued a Class 1 recall of all sizes of the cranial implant kit distributed from November 5, 2007 through October 23, 2008. The company is recalling these products because sterility cannot be assured.
     
 

The FDA has reported that many typical and atypical antipsychotic medications as well as SSRI antidepressants may cause Tardive Dyskinesia. Also drugs containing metoclopramide such as Reglan have been linked to cases of Tardive Dyskinesia.

     
  Toyota & Lexus Floor Mat Recall:
Toyota Motors has issued a recall of floor mats installed in certain Toyota and Lexus vehicles due to a problem with the mats getting stuck under the accelerator pedal resulting in serious injury or death.
     
Trasylol   Recent studies have linked Trasylol to an increased risk of kidney damage, heart attacks, and strokes.
Breaking News....FDA Halts Trasylol Sales Due To Higher Death Risks
   
Yaz Side Effects   Yaz, Yasmin, and the generic form Ocella are a type of birth control that have been linked to serious side effects such as heart attack, blood clots, stroke, and death among other adverse effects.
     
Zimmer Durom Cup Hip Implant   Sales of the Zimmer Durom Cup hip replacement have been suspended in the United States since many doctors have reported a substantially higher need for revisions and further hip surgery.
     
Zicam Side Effects Lawyer  

Zicam Cold Remedy Recall Lawsuit:
Zicam has recently been recalled du to several reports of users experiencing permanent loss of smell and taste after using Zicam Nasal Gel and Zicam Nasal Swabs products.

     
Ford Fire Recalls   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 flame. Click here to learn more about the Ford Fire Recalls.
   
Bard Composix Kugel Hernia Repair Patch   Bard Composix Kugel Hernia Repair Patches were recalled in March, 2006 due to a design flaw that may allow the memory recoil ring to break, causing problems such as bowel perforation.
Recently there has been an addition to the already recalled hernia patches
     
  Polaris All-Terrain Vehicle's (ATV) manufactured from mid 2004-2005 have been recalled. The recall is due to faulty electronic control modules which may overheat and cause a fire. ***Breaking News*** In July 2009 Polaris also recalled 2009 Sportsman models due to fire and burn risks.
     
Yamaha Rhino   Yamaha Rhino Rollover Accidents are being reported more frequently due to several design flaws. Though Yamaha is aware of the design flaws, a formal Yamaha Rhino recall has not been issued.
     
Shoulder Pain Pump Lawsuit   Shoulder Pain pumps are used to deliver pain medication to the shoulder following arthoscopic shoulder surgery. Recently they have been linked to cases of Postarthroscopic Glenohumeral Chondrolysis also know as PAGCL.
     
Smith & Nephew Knee Replacement   Smith & Nephew Oxinium Cementless Knee Replacements have a design defect that may cause injury. If you have been injured as a result of Smith & Nephew knee replacement, you may be entitled to compensation.
     
Stryker Hip Implant   Stryker Hip Implants have recalled two if its hip implant components that may cause injury. If you have been injured as a result of Stryker hip implant, you may be entitled to compensation.
     
ReliOn Insulin Syringe Recall   ReliOn Insulin Syringes have been recalled due to mislabeling. Some of the syringes labeled as U-40 are actually U-100 syringes and use of the mislabled syringes may cause serious injury or even death.

 

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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