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    Manufacturers of prescription drugs have a duty to patients to produce safe products, and to warn patients and their doctors of any adverse health effects.

    If you or a loved one were just injured, you should not feel pressured to make an immediate decision about hiring counsel. Focusing on restoring your health or mourning the loss of loved ones should take precedence over liability issues at this difficult time. However, keep in mind that each state imposes a deadline for filing lawsuits. This deadline is known as the statute of limitations.

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    The pharmaceutical industry is both increasingly competitive and increasingly profitable.

    Drug makers manufacture their products often for global markets and in certain cases minimize risks associated with their products through warning labels in order to expedite their release. Drug makers also sometimes fail to sufficiently test their products before releasing to the public. In the end the consumers suffer and are in some cases suffered severe health complications including heart attack, stroke, pulmonary embolism, diabetes, adrenal failure and even death.

    " If you or a loved one have been prescribed any of the pharmaceutical drugs on this website and have suffered side effects you contact us for a free case evaluation immediately. "

    FDA Drug Recalls
  • Federal Recalls and Warning Letters

    The resources available are provided to offer information to protect consumer safety.

    We closely follow updates released by the U.S. Food and Drug Administration (FDA), a federal agency in the Department of Health and Human Services. Some of the most recent alerts are:

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    If you or a loved one has been the victim of a drug recall or suffered serious side effects from using any of these drugs or devices, we can help. You may be eligible for even larger compensation than you think. Know your legal rights.

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Hernia Mesh LAWSUIT

If you had a hernia mesh repair surgery that used a brand of mesh called Ethicon Physiomesh or Atrium C-Qur, you could be at risk. Any pain, bleeding, infection, or other symptoms you suffer could be the result of hernia mesh failure.
Hernia Mesh Complications:
  • Pain
  • Swelling
  • Mesh Migration
  • Bacterial infections
  • Hernia recurrence

3M Earplugs WARNING

If you were issued earplugs, suffered hearing loss and served anytime between 2003 to 2015, you may qualify for a one-time hearing loss pay out.
Veterans and active military who used the defective 3M earplug may be suffering from various symptoms, including:
  • Tinnitus (ringing in the ears)
  • Muffling of speech
  • Trouble hearing consonants
  • Withdrawal from conversations
  • Need for increased volume on TV and radio


Retrievable IVC Filters, including the C.R. Bard's (unit of Johnson & Johnson) Recovery IVC Filter and C.R. Bard’s G2 IVC Filter System, have reportedly been fracturing and migrating inside of patients, leading to serious injuries, including perforation of the interior vena cava (IVC).
IVC filters being investigated:
  • B Braun Tempofilter IVC filter (retrievable)
  • Bard G2x IVC (retrievable, unlimited indwell time)
  • Bard G2 (retrievable)
  • Cook Günther Tulip (retrievable)
  • Cook Celect (retrievable)
  • Cordis OptEase IVC filter (retrievable, 23 day indwell time)
  • ALN IVC filter (retrievable)
  • Rex Medical Option IVC filter (retrievable)

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Recent Warnings

3M Company Agrees to Pay $9.1 Million to Resolve Allegations That it Supplied the United States With Defective Dual-Ended Combat Arms Earplugs

  • July 26, 2018

The Department of Justice announced today that 3M Company (3M), headquartered in St. Paul, Minnesota, has agreed to pay $9.1 million to resolve allegations that it knowingly sold the dual-ended Combat Arms Earplugs, Version 2 (CAEv2) to the United States military without disclosing defects that hampered the effectiveness of the hearing protection device.

(read more)
Health Blog

FDA Rejects Wider Use Of Xarelto Drug For A Third Time

  • February 14, 2014


The U.S. Food and Drug Administration have declined - for a third time - to approve proposed expanded use of Bayer AG and Johnson & Johnson's lucrative blood thinning drug, Reuters reported.

The drugmakers of Xarelto, a drug used to reduce dangerous blood clots and related problems in patients with coronary artery disease, sought approval from the U.S. regulators to market the pill for prevention "of new heart attacks and strokes, and death, in patients with acute coronary syndrome (ACS), and also to prevent clogging of heart stents," Reuters reported.

(read report)

Health Blog

New study adds caution to testosterone therapy for “low T”

  • January 31, 2014

Harvard Health Blog

Mass marketing of testosterone therapy may have men eager to try this seemingly simple fix. But the latest science should have them scratching their heads and putting away the credit card—at least for now.

A new study published in the online journal PLOS One shows an increase in the risk of having a heart attack in the months after starting testosterone therapy.

(read blog)

Medical Alerts

Food and Drug Administration
British Medical Journal
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