What to Know about Wrongful Death Claims

Losing a loved one in an accident caused by someone else’s negligence is an unimaginable tragedy, leaving families overwhelmed with grief and uncertainty. Filing a wrongful death claim

In Maryland, the law recognizes the profound impact of such a loss and provides a way for families to seek justice through the Maryland Wrongful Death Statute.

When faced with the wrongful death of a loved one, understanding how this law works, who it protects, and how it can help families hold negligent parties accountable is important.

If you have questions about the untimely death of a loved one in an accident, contact an experienced wrongful death lawyer.

wrongful death lawyer in Maryland

Why file a wrongful death claim?

Filing a wrongful death claim can be a vital step for families seeking justice after losing a loved one due to someone else’s negligence. This legal action allows surviving family members to hold the responsible party accountable and recover compensation for the emotional and financial hardships caused by their loss.

While no amount of money can replace a loved one, a wrongful death lawsuit can help ease the burden of:

–      medical expenses

–      funeral costs

–      lost income

–      provides some stability and support during an incredibly difficult time.

It’s also a way to honor your loved one’s memory by ensuring that negligence doesn’t go unanswered.

wrongful death attorneys near me

What are Maryland’s wrongful death statutes?

Wrongful death statutes play a crucial role in personal injury cases by equalizing the opportunity for surviving family members to obtain justice, whether the harm caused by a defendant’s negligence or wrongful act results in death or injury.

Originally, surviving family members had no legal remedy for the loss of a loved one caused by a defendant’s harmful act.

This limitation created the innuendo that it was cheaper for defendants to cause death over injury. Fortunately, this problem was remedied in 1852 with the passage of the Maryland Wrongful Death Act by the Maryland Legislature.

Currently codified at § 3-901 of the Courts and Judicial Proceedings Article in the Maryland Code, a cause of action – separate from a personal injury claim – is provided for certain family members of a deceased individual.

Essentially, Maryland’s wrongful death statute grants the decedent’s surviving family members the right to sue for compensation for the loss if another person’s negligence caused the death.

unlawful death lawyers

Who has the right to file a wrongful death claim?

The determination of which family members are eligible to file a wrongful death claim is explained in § 3-904 of the statute. Eligible parties are categorized into primary versus secondary beneficiaries.

Primary beneficiaries are the decedent’s spouse, parents, and children, as they are viewed to have suffered the most direct harm and impact from the loss of a loved one.

Secondary beneficiaries are financially dependent family members, such as siblings, relatives, or individuals related by marriage to the decedent.

Evidence documenting (or illustrating) the close relationship to the decedent is required for secondary beneficiaries to show a strong dependency on the loved one and the negative impact of the loss.

Understanding Statutes of Limitations for Maryland Wrongful Death Cases

Statutes of limitations set forth clear time frames for eligible parties to bring forth a cause of action.

For a Maryland wrongful death claim, the statute of limitations is within three years of the decedent’s death. Failing to adhere to this time frame will typically result in a complete and final bar of the claim.

Importantly, wrongful death actions are not derivative claims to recover for the harm that the decedent experienced prior to his or her death.

Instead, wrongful death actions are for the surviving family members who have experienced the loss of their loved one. It is a claim that is separate and apart from the decedent’s own claim before his or her death.

Thus, even if the statute of limitations has passed for the decedent’s claim, family members can still pursue an independent wrongful death claim within the time frame of three years from the date of the decedent’s death.

Are Funeral Costs and Emotional Loss Covered in a Wrongful Death Claim?

The purpose of wrongful death claims is to compensate designated surviving family members for the harm they have experienced from the loss of their loved one.

Economic damages compensate beneficiaries for calculable losses due to the death of a loved one and include costs such as funeral expenses and the loss of the decedent’s expected earnings, financial contributions, and benefits.

Non-economic damages refer to the intangible harm that beneficiaries experience from the loss of their loved one, such as pain and suffering, grief, loss of companionship, emotional support, and consortium.

Due to the non-quantifiable nature of non-economic damages, Maryland juries are instructed to allocate a reasonable figure (within the state cap of $920,000 for non-economic damages) for the beneficiaries’ emotional suffering.

Did Negligence Cause a Loved One’s Death?

Wrongful death can result from a wide range of accidents caused by negligence or wrongful actions.

Car Accident Deaths: These can include motor vehicle accidents, such as car, truck, or motorcycle crashes, where reckless driving, speeding, or impaired driving leads to fatal injuries.

Workplace Accident Deaths: Workplace accidents, particularly in hazardous industries like construction, can also result in wrongful death if safety protocols are ignored.

Medical Negligence Deaths: Medical malpractice, including misdiagnosis, surgical errors, or birth injuries, is another common cause.

Defective Product Deaths: Product defects, such as faulty machinery or dangerous consumer goods, can tragically lead to loss of life.

In all these cases, the common thread is negligence or misconduct that could have been prevented, making it possible for surviving family members to seek justice and accountability. It is important to hire a personal injury attorney who knows wrongful death law.

Understanding Estate Claims and Wrongful Death in Maryland

Often confused with wrongful death beneficiaries, are intestate law beneficiaries or beneficiaries named in a will. However, there are key differences between wrongful death claims and estate claims.

Notably, wrongful death claims grant family members the right to bring legal action for the harm they experienced from the loss of their loved one due to negligence or a “wrongful” act. The beneficiaries outlined in the statute receive compensation for their losses.

In contrast, any (settlement) funds obtained are subject to legal directives from the decedent’s will or, if there is no will, as per Maryland’s intestacy laws.

While an individual may not be entitled to recovery from a wrongful death claim per the wrongful death statute in Maryland, they may be able to recover damages awarded to the estate from the decedent’s survival action if the person’s share is identified in the will.

In the absence of a will, the allocation of funds will be determined by Maryland’s intestacy laws.

Maryland’s Trusted Wrongful Death Lawyers

At The Yost Legal Group, we understand the overwhelming pain and challenges families face after the untimely loss of a loved one due to someone else’s negligence.

Our personal injury law attorneys are dedicated to helping individuals in Maryland protect their rights. We work to pursue full compensation to ease the financial and emotional burdens of such a devastating loss.

Our compassionate wrongful death attorneys will guide you every step of the way. Cases are handled on a contingency fee basis. When we file a lawsuit in Maryland, you do not have to pay any upfront money. We are paid after we settle your case.

If you have lost a loved one and have questions, contact The Yost Legal Group today. We provide a free case review, so call (800)-YOST-LAW, (800)-967-8529.

You don’t have to face this alone—we’re here to help. It is essential to know your legal options.

Lawyers for Wrongful Death – Lawyer for Personal Injury – Lawyer for Truck Accident

Unlawful Death Lawyers – Bicycle Injury Lawyer – Motorcycle Accident Lawyer

Optetrak Patella Implant Device Exactech Recall

A letter was recently sent to surgeons, hospitals, and healthcare professionals announcing the voluntary recall of the Exactech Optetrak Patella implant device.

The voluntary Exactech recall concerns Patella lots that were packaged without the ethylene vinyl alcohol (EVOH) layer. Experts advised doctors not to implant these potentially harmful devices packaged in faulty packaging.

Medical professionals were advised to stop using the product immediately and set aside any that might be affected. They were instructed that healthcare professionals should report any adverse reactions or noticeable quality issues as patients come forward.

Our attorneys handle Exactech recall lawsuits nationwide. If you’ve experienced failure of an Exactech knee, hip, or ankle implant that was recalled, leading to revision surgery, we’re here to help.

Stay informed with the latest updates and insights on this page.

Don’t overlook your rights—contact our product liability lawyers at 800-967-8529 or online. You won’t incur any fees unless you receive financial compensation.

Exactech Optetrak Patella recalled medical device

Exachtech Addresses Oxidation Risk with Packaging Recall

From 2004 to August 2021, Exachtech used two types of packaging materials in its process: (1) Low-Density Polyethylene (LDPE), Nylon, and EVOH, or (2) LDPE and Nylon without EVOH.

EVOH improves the prevention of oxygen permeation. Thousands of devices were packaged without using an EVOH oxygen barrier layer, which potentially causes unintended oxidation and early degradation of the affected device.

Given the potential for oxidation-related issues, Exachtech voluntarily recalled these lots as a precautionary measure.

The recall emphasizes the importance of surgeons regularly monitoring patients with affected devices for signs of wear and failure. The crucial issue is determining how many thousands of patients might suffer from device-related pain or failure, potentially needing revision surgery.

knee replacement recall lawsuit by The Yost Legal Group

Stay Informed on Patella Device Recall and Risks

The lot-specific voluntary recall relates to Patella devices manufactured from 2004 through August 2021. These devices were marketed as Optetrak and cleared through 510(k): K932690, K933610, and K160484.

All healthcare professionals were instructed to review the following information and take any necessary actions. Then, the information advised diagnostic considerations, such as performing X-rays to evaluate the patient further if device failure is suspected.

Potential issues due to oxidation include:

–             Accelerated device wear or failure

–             Component cracking or fracture

–             New or worsening pain

–             Bone loss

–             Swelling in the affected area

Key Information on Optetrak Device Failures

The recall names all of these knee replacement devices, which could necessitate revision surgery for patients.

Part Number Device Description                                                         Device Identifier

200-02-26        THREE PEG PATELLA 26MM                                    10885862039576

200-02-29        THREE PEG PATELLA 29MM                                    10885862039583

200-02-32        THREE PEG PATELLA 32MM                                    10885862039590

200-02-35        THREE PEG PATELLA 35MM                                    10885862039606

200-02-38        THREE PEG PATELLA 38MM                                    10885862039613

200-02-41        THREE PEG PATELLA 41MM                                      10885862039620

200-03-26        ONE PEG PATELLA 26MM                                         10885862039637

200-03-29        ONE PEG PATELLA 29MM                                         10885862039644

200-03-32        ONE PEG PATELLA 32MM                                         10885862039651

200-03-35        ONE PEG PATELLA 35MM                                         10885862039668

200-03-38        ONE PEG PATELLA 38MM                                         10885862039675

200-03-41        ONE PEG PATELLA 41MM                                          10885862039682

200-05-23        INSET PATELLA 23MM                                              10885862039835

200-05-26        INSET PATELLA 26MM                                               10885862039842

200-05-29        INSET PATELLA 29MM                                               10885862039859

200-07-26        ADVANCED PATELLA 26MM 3 PEG IMPLANT  10885862314260

200-07-29        ADVANCED PATELLA 29M 3 PEG IMPLANT      10885862314277

200-07-32        ADVANCED PATELLA 32MM 3 PEG IMPLANT  10885862314284

200-07-35        ADVANCED PATELLA 35MM 3 PEG IMPLANT  10885862314291

200-07-38        ADVANCED PATELLA 38MM 3 PEG IMPLANT  10885862314307

Exactech lawsuits by The Yost Legal Group

The Hidden Dangers of 510(k) Fast-Track FDA Approvals

Between 1994 and 2017, Exactech secured multiple 501(k) clearances from the FDA for its Optetrak, Optetrak Logic, and Truliant total knee replacement implant systems and components.

The FDA’s 510(k) clearance, known as “fast-track” approval, does not require manufacturers to prove a product’s safety and effectiveness.

This process, known as “premarket notification” or 510(k) clearance, only requires the manufacturer to demonstrate that the device is substantially equivalent to a pre-MDA predicate device.

Consequentially, the FDA can “clear” a new device for sale in the USA. Under the 510(k) process, the component parts used in the Exactech Optetrak Devices were either approved by the FDA or marketed without receiving either 510(k) clearance or full approval by the FDA.

Simply put, not enough product development and testing was done to ensure product safety. This can lead to patient harm and potential recalls, which is precisely what has happened.

Protect Your Rights Against Defective Medical Products

At Yost Legal Group, our priority is ensuring patient safety and achieving effective outcomes for patients with life-altering defective medical products. Our knee replacement lawsuit attorneys will help you file a lawsuit to seek compensation.

Collaborative efforts are essential for the success of actions against medical device manufacturers—especially those who continuously market harmful products.

Our law firm is dedicated to defending the rights of individuals against powerful corporations. Accordingly, when huge medical device manufacturers like Exactech continue to put profits before people, we step in to level the playing field.

Learn about your legal rights. We can file a product liability case on your behalf if you have a defective medical device. The Yost Legal Group is filing the current personal injury lawsuits:

  • Knee replacement recall
  • Shoulder replacement recall
  • Hip replacement recall
  • Exactech lawsuits

Empowering Patients, Challenging Corporations

If you or a loved one had knee replacement surgery in the past ten years and are experiencing pain, a clicking noise, swelling, or any other medical concerns, contact your doctor immediately.

Contact The Yost Legal Group for a free and confidential consultation at 1-800-967-8529. Our personal injury law firm is committed to promptly and transparently addressing potential concerns. If you had knee replacement surgery and are affected by the Exactech knee recall, please contact us.

Hold Exactech accountable for the harm they’ve caused. Our legal team is committed to seeking justice and ensuring they change their ways. A product defect lawyer will file an Exacteck lawsuit on your behalf.

For more information or to discuss your case, call us at 1-800-967-8529 or click this link to request an appointment.

By pursuing an Exactech knee replacement lawsuit, you will help send a powerful message for change. You may qualify for a significant financial recovery.

At The Yost Legal Group, you never have to pay anything upfront. We only get paid after we settle your case. If there is no recovery, no legal fees or expenses are due. Our personal injury law attorneys will provide legal representation with a free case evaluation.

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Consumers are encouraged to report any adverse events or quality concerns related to this recall to the FDA through the MedWatch reporting system. You can go online at the FDA Medwatch Website or call 1-800-FDA-0178.