Hollis Law Firm

Hollis Law Firm The Hollis Law Firm handles cases for people who have been injured by harmful prescriptions We are ready to listen to you. We are here to represent you.

The Hollis Law Firm handles cases for people who have been injured by harmful prescription drugs and medical devices, such as hernia mesh. Clients are represented on a contingent fee basis, which means that the client is not responsible for paying costs or fees unless there is a recovery. All aspects of the attorney-client relationship are kept strictly confidential. We take pride in the fact that

we respond to client inquiries and phone calls personally and promptly. From the firm’s offices in a suburb of Kansas City, Missouri, the firm has represented clients from all parts of Missouri, Kansas, Iowa, Nebraska, Minnesota, and has partnered with other law firms to serve clients throughout the U.S. Our lawyers want to help you get the results that you need to move forward with your life. Our philosophy is that we are your guides. After we take the time to understand your needs, we will provide you with the education you need to make the decisions. You will make the decisions and we will listen. We will take action on any choice you make. "Aggressive, effective legal representation with a personal touch."

FDA warns that certain Cook Medical Sizing Catheters should not be used due to risk of breaking.
04/14/2026

FDA warns that certain Cook Medical Sizing Catheters should not be used due to risk of breaking.

When the sizing catheters are used during angiographic procedures the marker bands may be at an increased risk of cracking/breakage.

"CEREPAK Detachable Coil Systems, reported failure to detach in some products."
02/09/2026

"CEREPAK Detachable Coil Systems, reported failure to detach in some products."

MedTech/CERENOVUS is removing CEREPAK Detachable Coil Systems due to a higher than expected failure to detach rate

Abbott reports update on FreeStyle Libre 3 Sensors, incorrect glucose readings.
02/05/2026

Abbott reports update on FreeStyle Libre 3 Sensors, incorrect glucose readings.

What is a Medical Device Recall?

"FDA approved reformulated ranitidine tablets."
12/03/2025

"FDA approved reformulated ranitidine tablets."

Today, the U.S. Food and Drug Administration approved reformulated ranitidine tablets, marking the return of this important acid-reducing medication to the U.S.

"Wearable device FreeStyle Libre 3 and Libre 3 Plus glucose monitoring sensors, risk inaccurate low glucose readings."
12/02/2025

"Wearable device FreeStyle Libre 3 and Libre 3 Plus glucose monitoring sensors, risk inaccurate low glucose readings."

Certain Abbott Diabetes Care Continuous Glucose Monitor sensors may provide incorrect low glucose readings

"FDA recalling the i-View Laryngoscope due to issues which may cause serious adverse consequences."
11/21/2025

"FDA recalling the i-View Laryngoscope due to issues which may cause serious adverse consequences."

Intersurgical is recalling the i-View Video Laryngoscope due to the device not turning on, battery liquid leakage and screen going blank.

FDA to recommend standard chocking protocol, says 'anti-chocking devices are not FDA authorized.'
11/13/2025

FDA to recommend standard chocking protocol, says 'anti-chocking devices are not FDA authorized.'

These choking rescue protocols include abdominal thrusts (also called the “Heimlich” maneuver) for children and adults but not anti-choking devices.

Team at UMass has built the first Artificial Neurons that can interface directly with living ones.
10/07/2025

Team at UMass has built the first Artificial Neurons that can interface directly with living ones.

A team of UMass Amherst engineers announced the creation of an artificial neuron with electrical functions that closely mirror those of biological ones.

"Certain lots of Medtronic Cannula Products: Catheter may not retain its shape."
09/16/2025

"Certain lots of Medtronic Cannula Products: Catheter may not retain its shape."

Medline is recalling certain Medline Kits containing recalled Medtronic DLP Left Heart Vent Catheters as the catheter may not retain its shape.

"Gamrozyne is only available by prescription from a licensed veterinarian because professional expertise is required to ...
08/28/2025

"Gamrozyne is only available by prescription from a licensed veterinarian because professional expertise is required to accurately diagnose BRD and monitor the safe and effective use of this product."

FDA Approves First Generic Gamithromycin Injectable for Treatment and Control of Bovine Respiratory Disease in Beef and Non-Lactating Dairy Cattle U.S. Food and Drug Administration sent this bulletin at 08/28/2025 10:19 AM EDT If your email program has trouble displaying this email, view as a webpag...

"There has been one death from encephalitis directly attributable to the vaccine'
08/25/2025

"There has been one death from encephalitis directly attributable to the vaccine'

On August 22, 2025,the US FDA’s Center for Biologics Evaluation and Research has suspended the biologics license for Valneva Austria GmbH’s Ixchiq (Chikungunya

"Class 1 Device Recall Carotid WALLSTENT Monorail Endoprosthesis."
08/22/2025

"Class 1 Device Recall Carotid WALLSTENT Monorail Endoprosthesis."

Boston Scientific Removes Carotid WALLSTENT Monorail Endoprosthesis due to risk of resistance during device withdrawal

Address

8101 College Boulevard Suite 260
Overland Park, KS
66210

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Telephone

+18007013672

Website

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