CATHETER DEFECTS
Defective Catheter Lawsuits
Investigating medical device recalls & catheter injury
Medical device manufacturers and the U.S. Food and Drug Administration (FDA) have both initiated recalls for defective catheters after medical reports of serious health complications linked to catheter defect and device failure.
Following injury, plaintiffs and product liability attorneys have filed claims against device manufacturers for alleged negligence, improper pre-market testing, and distributing unsafe medical devices.
Defective catheters have been recalled for separation risks, breakage, and perforating blood vessels, leading to serious injury and death. Catheters are most commonly recalled after causing complications during medical procedures like administering medication, injecting contrast dye, and removing blood clots.
When a catheter is defective, it may not function as intended, and may not drain fluids as designed, causing serious health problems. Broken catheters or separating catheters can lead to fragments of the device left in a patient’s body or bloodstream.
Joe Lyon is an experienced medical device defect lawyer and product liability attorney investigating injury claims linked to defective catheters for plaintiffs nationwide.
Catheter Recalls
- Cook Medical Catheter
- Boston Scientific Fetch 2 Aspiration Catheter
- Innervision Snap Shunt Ventricular Catheter
- BioGlide and Snap Shunt Ventricular Catheter
- Angiodynamics Soft Vu Omni Flush Angiographic Catheters
- Vascular Solutions Twin-Pass Dual Access Catheters
- Abbott POWERSAIL® Coronary Dilatation Catheters
- Acclarent Inspira AIR Balloon Dilation System
- AngioSculpt EX Percutaneous Transluminal Coronary Angioplasty (PTCA) catheters
- Multi-Med Single Lumen Catheters
- Fire Star RX and Dura Star RX coronary balloon catheters
- OriGen Biomedical OriGen
- Penumbra Catheters
- Spectranetics Catheter
- Teleflex Medical Arrow Arterial Embolectomy Catheter
- Cook Medical Transseptal Needles
Patient Injury & Catheter Defects
Some common injuries reported in defective catheter adverse events can include:
- Heart attack
- Blood clot
- Organ damage
- Emergency surgery
- Death
- Air embolism
- Blood loss
- Cardiac arrest
- Infection
Defective Catheters & Medical Device Litigation
Due to longstanding loopholes in the FDA medical device approval process, many defective medical products injure patients each year. As a result, injured plaintiffs and product liability attorneys are forcing medical device companies to claim responsibility and compensate those affected.
The Lyon Firm works with medical experts to determine the root cause of a medical injury, and reviews defective medical device recalls for injured plaintiffs nationwide.
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ABOUT THE LYON FIRM
Joseph Lyon has 17 years of experience representing individuals in complex litigation matters. He has represented individuals in every state against many of the largest companies in the world.
The Firm focuses on single-event civil cases and class actions involving corporate neglect & fraud, toxic exposure, product defects & recalls, medical malpractice, and invasion of privacy.
NO COST UNLESS WE WIN
The Firm offers contingency fees, advancing all costs of the litigation, and accepting the full financial risk, allowing our clients full access to the legal system while reducing the financial stress while they focus on their healthcare and financial needs.

Why are these cases important?
When medical devices malfunction, the consequences can be devastating. Filing a lawsuit ensures victims are compensated for medical bills, lost income, and ongoing care. More importantly, it holds manufacturers accountable, forcing them to take responsibility for negligence. These lawsuits often lead to safer products and stricter oversight. Choosing to file isn’t just about personal recovery—it’s also about making healthcare safer for future patients nationwide.
CONTACT THE LYON FIRM TODAY
Questions about Defective Catheter Litigation
If a device breaks or fails, patients may suffer from internal bleeding, embolisms, revision surgery, organ damage or death.
When a catheter has the potential to fail and cause injury, companies should voluntarily issue a recall. When a company injures patients with defective medical devices, a product liability lawyer may help you recover financial losses, medical expenses and other damages incurred through litigation.
- Medtronic
- Cook Medical
- Boston Scientific
- Bard
- Abbott Vascular
- Edwards Lifesciences
- Merit Medical Systems
- ReFlow Medical
- Stryker
- Sterilmed
- Teleflex
- Terumo Medical
Defining a medical device as defective involves analyzing whether it performs as safely as consumers reasonably expect. Three primary types of defects exist: design, manufacturing, and marketing. A design defect makes the entire product inherently unsafe, such as flawed pacemaker circuitry. A manufacturing defect occurs when an otherwise safe device is produced incorrectly, like a contaminated surgical instrument. Marketing defects involve missing warnings or unclear instructions. Regulatory approval alone does not shield manufacturers from liability. If patients suffer harm while using the product as intended, courts may label the device defective, opening the door for legal accountability.
The Lyon Firm is the right choice if you want a lawyer who combines national trial experience with a personal touch. Joe Lyon has handled high-profile cases involving dangerous drugs, defective products, and toxic workplace exposures. He understands how overwhelming the legal process can feel and ensures clients stay informed at every stage. The firm is known for its client-centered approach—treating cases not as files, but as real people’s stories. With a history of winning significant settlements and verdicts, The Lyon Firm offers proven results and genuine compassion, making it a trusted advocate for those facing legal challenges.
Learn about Medical Device Approval Processes
Medical Device Information Center
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