Fitzgerald Law Group, LLC

Directions Website Contact the business

Fitzgerald Law Group, LLC Medical device, prescription drug and consumer product injury attorneys.

In February 2026, Bayer and Monsanto announced a proposed $7.25 billion national settlement designed to resolve both cur...
09/17/2026

In February 2026, Bayer and Monsanto announced a proposed $7.25 billion national settlement designed to resolve both current and future Roundup claims. Individuals who used Roundup and were or are diagnosed with non-Hodgkin’s lymphoma cancer can qualify for payouts ranging up to $165,000 depending on factors including whether exposure was residential or commercial, age at diagnosis, cancer severity, and types of cancer treatment. Fitzgerald Law Group has over 20 year’s experience handling complex product liability, medical device, and prescription drug injury cases. If you or a loved one used Roundup and has been diagnosed with non-Hodgkin’s lymphoma or one of its many subtypes, and want to know if you qualify for the proposed settlement, contact our Portland, Maine office at (207) 874-7407 or [email protected] or click the button below for a free, confidential claim evaluation.

On October 31, 2024, Cartiva, Inc. issued an urgent FDA Class II Device Recall of the Cartiva Synthetic Cartilage Toe Im...
04/16/2025

On October 31, 2024, Cartiva, Inc. issued an urgent FDA Class II Device Recall of the Cartiva Synthetic Cartilage Toe Implant sold from July 2016 to October 2024. The FDA Recall was necessary due to a higher-than-expected rate of serious injuries including pain, nerve damage, implant subsidence and fragmentation, and the need for revision or toe fusion surgery. Patients who have been implanted with the Cartiva Synthetic Cartilage Toe Implant may have a claim for injuries including pain and suffering, medical expenses, lost wages, and other damages. Our firm has over 20 years’ experience handling complex medical device injury cases. For a confidential claim evaluation, send us a message below or contact our Portland, Maine office at (207) 874-7407 or [email protected].

Depo-Provera is an injectable contraceptive manufactured by Pfizer that is administered every 3 months. Recent studies s...
10/17/2024

Depo-Provera is an injectable contraceptive manufactured by Pfizer that is administered every 3 months. Recent studies suggest that Depo-Provera may increase the risk of brain tumors called meningiomas which grow in the protective layers around the brain and spinal cord. Women who have used Depo-Provera and developed a meningioma may have a claim against Pfizer for pain and suffering, medical expenses, lost wages, and other damages. Our firm has over 20 years’ experience handling complex prescription drug injury cases for injured Mainers. For a confidential claim evaluation, send us a message below or contact our Portland, Maine office at (207) 874-7407 or [email protected].

The FDA has indicated that Covidien Hernia Mesh devices may be linked to serious complications including pain, mesh migr...
10/03/2024

The FDA has indicated that Covidien Hernia Mesh devices may be linked to serious complications including pain, mesh migration/tearing/shrinkage, hernia recurrence, infection, adhesions, and bowel obstruction. Covidien Hernia Mesh has been implanted at hospitals throughout Maine including Central Maine Medical Cener (CMMC), St. Mary’s Regional, and Maine General Medical Center (MGMC). Patient who have developed complications from a Covidien Hernia Mesh may be entitled to significant compensation including pain and suffering, medical expenses, and lost wages. Our firm has over 20 years’ experience handling complex medical device failure cases for injured Mainers. For a confidential case evaluation, send us a message below or contact our Portland, Maine office at (207) 874-7407 or [email protected].

Recent studies have linked the popular diabetes and weight loss drugs Ozempic, Wegovy, and Rybelsus with an increased ri...
07/31/2024

Recent studies have linked the popular diabetes and weight loss drugs Ozempic, Wegovy, and Rybelsus with an increased risk of developing gastroparesis or stomach paralysis and a serious eye condition known as non-arteritic anterior ischemic optic neuropathy (NAION) which can lead to sudden blindness. Patients who have used one of these medications and suffered gastrointestinal complications or vision impairment or loss may be entitled to significant compensation including pain and suffering, reimbursement of medical expenses, and lost wages. Our firm has over 20 years’ experience handling complex prescription drug injury cases for injured Mainers. For a confidential claim evaluation, send us a message below or contact our Portland, Maine office at (207) 874-7407 or [email protected].

HIP & KNEE IMPLANT FAILURE DUE TO POLYETHYLENE WEAR: In 2021, Exactech, Inc. issued FDA Recalls of over 200,000 hip and ...
05/10/2024

HIP & KNEE IMPLANT FAILURE DUE TO POLYETHYLENE WEAR: In 2021, Exactech, Inc. issued FDA Recalls of over 200,000 hip and knee implants due to the risk of polyethylene liner wear which can result in significant pain, bone damage, and revision surgery. Patients who underwent a hip or knee replacement surgery in Lewiston, Maine after 2010 and have experienced pain, swelling, or other symptoms may be entitled to significant compensation including reimbursement of the cost of revision surgery and out-of-pocket expenses. Our firm has over 20 years’ experience handling complex medical device failure cases for injured Mainers. For a confidential claim evaluation, send us a message below or contact our Portland, Maine office at (207) 874-7407 or [email protected].

SUBOXONE & TOOTH DECAY: U.S. drug companies created the opioid crisis that has ravaged this nation. Through the introduc...
01/24/2024

SUBOXONE & TOOTH DECAY: U.S. drug companies created the opioid crisis that has ravaged this nation. Through the introduction of drugs to treat opioid addition such as Suboxone, that same industry has profited from the devastation it wrought on victims of this epidemic. In 2022, the FDA issued a Drug Safety Alert warning that dental problems including tooth loss and decay have been reported with medications used to treat opioid addiction including Suboxone. Patients who have used Suboxone and suffered dental problems may be entitled to compensation. In December 2023, our firm filed the first Suboxone product liability case in Maine. To speak with an experienced Maine attorney about a potential Suboxone claim, click the link below to message our office or call (207) 874-7407 for more information.

The Paragard IUD is the only hormone free contraceptive device currently available in the U.S. Because the Paragard IUD ...
11/21/2023

The Paragard IUD is the only hormone free contraceptive device currently available in the U.S. Because the Paragard IUD does not contain hormones, many women have preferred its use without having to worry about hormone related side effects. However, increasing numbers of women are suffering breakage of one or more arms off the Paragard IUD prior to or during removal of the device. Women who have suffered breakage of the Paragard IUD may be entitled to significant compensation for their injuries. Our firm has over 20 years’ experience handling complex medical device failure cases for injured Mainers. For a free and confidential claim evaluation, send us a message below or contact our Portland, Maine office at (207) 874-7407 or [email protected].

HIP & KNEE REPLACEMENT FAILURE DUE TO PLASTIC WEAR & LOOSENING: In 2021, Exactech, Inc. issued FDA Recalls of over 200,0...
05/22/2023

HIP & KNEE REPLACEMENT FAILURE DUE TO PLASTIC WEAR & LOOSENING: In 2021, Exactech, Inc. issued FDA Recalls of over 200,000 hip and knee implants due to the risk of polyethylene liner wear which can result in significant pain, loosening, bone damage, and revision surgery. Patients who underwent a hip or knee replacement surgery after 2007 and have experienced pain, immobility, or other symptoms may be entitled to significant compensation including reimbursement of the cost of revision surgery and out-of-pocket expenses. Our firm has over 20 years’ experience handling complex medical device failure cases for injured Mainers. For a free and confidential claim evaluation, send us a message below or contact our Portland, Maine office at (207) 874-7407 or [email protected].

FDA RECALL OF EXACTECH PLASTIC LINERS: In 2021, Exactech, Inc. issued FDA Class 2 Device Recalls of over 200,000 hip and...
11/14/2022

FDA RECALL OF EXACTECH PLASTIC LINERS: In 2021, Exactech, Inc. issued FDA Class 2 Device Recalls of over 200,000 hip and knee implants due to the risk of polyethylene liner wear which can result in significant pain, bone and tissue damage, loosening, and the need for revision surgery. Patients who underwent a hip or knee replacement surgery at a Lewiston, Maine hospital after 2007 and who have experienced pain, immobility, or other symptoms may be entitled to significant compensation including reimbursement of the cost of revision surgery and out-of-pocket medical expenses. Our firm has over 20 years experience handling complex medical device failure cases for injured Mainers. For a free and confidential claim evaluation, contact our Portland, Maine office at (207) 874-7407 or [email protected].

Address

120 Exchange Street, Suite 200
Portland, ME
04101

Opening Hours

Monday 9am - 6pm
Tuesday 9am - 6pm
Wednesday 9am - 6pm
Thursday 9am - 6pm
Friday 9am - 6pm

Website

Alerts

Be the first to know and let us send you an email when Fitzgerald Law Group, LLC posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Business

Send a message to Fitzgerald Law Group, LLC:

Shortcuts

Share

Category