Why Choose Goza & Honnold?
Surgical staplers are used in a wide range of medical procedures to connect, seal, or divide tissue. When these devices function properly, they can help surgeons perform complex operations efficiently.
However, surgical stapler malfunctions and complications involving surgical staples have raised serious patient safety concerns.
Problems involving improperly formed staples, device misfires, or failures to seal tissue may contribute to severe bleeding, infection, additional surgeries, and other potentially life-threatening complications.
At Goza & Honnold, LLC, our Kansas City defective medical device attorneys have experience handling complex product liability claims involving allegedly dangerous medical products.
Our firm serves individuals and families throughout Kansas, Missouri, and beyond who have questions about injuries potentially connected to surgical staplers and staples.
Surgical staplers are medical devices used to close incisions, connect tissue, or cut and seal tissue during certain surgical procedures.
They may be used in operations involving the digestive tract, lungs, and other parts of the body.
Common procedures that may involve surgical staplers include:
Surgical staplers and the staples they deploy are separate medical products, and the FDA regulates them under different requirements.
Some staples are designed to remain inside the body permanently, while others are used externally and removed after healing.
Surgical staplers are designed to place staples precisely and, in some procedures, cut tissue at the same time.
When a device fails to operate as intended, serious complications may occur.
Potential problems include:
A stapler may fail to deploy staples correctly or may not complete its intended firing sequence.
Depending on the circumstances, this can leave tissue inadequately closed or sealed.
Staples may not form correctly, potentially preventing tissue from being securely connected.
Improper staple formation may contribute to bleeding or leakage.
If a stapled connection does not hold properly, fluids or contents from an organ may leak into surrounding tissue.
This can be particularly serious in gastrointestinal procedures.
Mechanical problems involving the stapler or its components may interfere with proper operation.
Complications may also occur when an inappropriate device or staple size is selected for the tissue involved.
Some of these situations may involve product defects, while others may raise questions about surgical technique, training, or medical judgment.
Determining the cause of a complication requires careful investigation.
Complications involving surgical staplers and staples can range from treatable postoperative problems to life-threatening injuries.
Potential injuries include:
A stapler malfunction or failure to properly secure tissue may contribute to bleeding during or after surgery.
Severe bleeding can require emergency treatment, blood transfusions, or additional surgery.
If a stapled connection fails, bacteria or other contents may escape into surrounding areas.
In some circumstances, this can lead to serious infection or sepsis, a life-threatening response to infection.
A fistula is an abnormal connection between organs or tissues.
Surgical leaks and fistulas can develop following certain gastrointestinal procedures and may require extensive treatment.
Improper stapling, device malfunction, or other complications may cause injury to surrounding tissue or organs.
Not every complication following stapler use establishes that the device was defective.
The U.S. Food and Drug Administration has issued safety communications addressing problems associated with surgical staplers and implantable staples.
In 2019, the FDA reported receiving more than 41,000 medical device reports involving surgical staplers and staples for internal use between January 1, 2011, and March 31, 2018.
Those reports included approximately:
The reports raised concerns about problems such as improper staple formation, device misfires, difficulty firing, and failure to deploy staples.
These figures represent adverse event reports, not confirmed findings that every injury or death was caused by a defective surgical stapler.
Adverse event reporting can help regulators identify potential safety problems, but the reports alone cannot establish how frequently a complication occurs or determine legal responsibility.
Following concerns about surgical stapler safety, the FDA took additional regulatory steps involving these devices.
In 2019, the agency issued recommendations to health care professionals regarding the safe use of surgical staplers and staples for internal use.
The FDA also moved to strengthen oversight of surgical staplers, including reclassifying certain surgical staplers from Class I to Class II medical devices.
This change established additional regulatory controls intended to address safety and effectiveness.
Certain surgical stapler products have also been subject to recalls or other corrective actions.
A recall may involve a specific manufacturer, device model, production lot, or identified safety issue.
A recall does not necessarily mean that every product made by a manufacturer is defective, and the absence of a recall does not automatically rule out a potential legal claim.
Surgical stapler safety concerns have involved products from multiple medical device manufacturers.
Manufacturers associated with surgical stapler products include:
The relevance of a particular manufacturer depends on the device used during surgery, its model, the circumstances of the complication, and available evidence.
An attorney may need to review hospital purchasing records, operative reports, and device identification information to determine which product was involved.
If you or a loved one experienced a serious complication following surgery involving a surgical stapler, you may have questions about whether a legal claim is available.
Factors an attorney may evaluate include:
Not every surgical complication supports a product liability lawsuit.
An attorney can help determine whether further investigation may be appropriate.
The circumstances surrounding a surgical stapler injury may involve different legal issues.
A product liability claim may involve allegations that a surgical stapler or staple was defectively designed, improperly manufactured, or accompanied by inadequate warnings or instructions.
Depending on the circumstances, a manufacturer or another legally responsible party may be involved.
Some injuries may result from improper device selection, surgical technique, or other alleged departures from the applicable standard of medical care.
These situations may involve medical malpractice rather than a defective product.
In some cases, a surgical complication may involve questions about both the device and the way it was used.
Determining responsibility often requires medical records, technical evidence, and expert review.
Surgical stapler claims often involve complicated medical and technical questions.
Potentially relevant evidence includes:
In some cases, expert testimony may be necessary to evaluate whether a device malfunctioned and whether that malfunction contributed to the injury.
Depending on the circumstances and applicable law, damages in a successful surgical stapler injury claim may include:
Costs associated with emergency treatment, additional surgeries, hospitalization, rehabilitation, and ongoing medical care.
Wages lost during recovery and, where supported by the evidence, diminished future earning capacity.
Depending on applicable law, compensation may be available for physical pain, emotional distress, permanent limitations, and reduced quality of life.
When a qualifying injury results in death, eligible family members or representatives may have questions about a potential wrongful death claim.
The availability and amount of compensation depend on the individual facts and applicable law.
No particular outcome can be guaranteed.
Goza & Honnold’s attorneys have decades of experience handling complex litigation involving medical devices, pharmaceuticals, and allegedly defective products.
Members of our legal team previously represented corporate defendants in complex product liability litigation.
That background provides insight into how medical device manufacturers and opposing counsel may investigate and defend claims.
A serious surgical injury can create unexpected medical expenses, prolonged recovery, and lasting physical limitations.
Our attorneys take the time to understand the circumstances, evaluate relevant evidence, and explain the legal options that may apply.
Possibly.
A documented malfunction may be important evidence, but a viable claim also depends on the nature of the injury, whether the malfunction contributed to it, and applicable legal requirements.
Additional surgery may be relevant to evaluating a potential claim.
However, the reason for the complication must be investigated before determining whether a manufacturer or medical professional may be legally responsible.
No. A recall is not necessarily required for a product liability claim.
Likewise, a recall does not automatically establish that a device caused an individual’s injury.
No.
A defective medical device claim generally focuses on alleged problems with the product, while a medical malpractice claim focuses on whether a health care professional met the applicable standard of care.
Some cases may involve both types of questions.
Filing deadlines depend on the circumstances and applicable state law.
Because evidence can become more difficult to obtain over time, prompt legal evaluation may be important.
Goza & Honnold serves clients throughout the Kansas City metropolitan area, including Kansas City, Kansas; Kansas City, Missouri; Overland Park; Johnson County; and surrounding communities.
Our attorneys also handle select complex medical device litigation matters beyond Kansas and Missouri.
Whether you are researching a Kansas surgical stapler lawsuit or a Missouri defective medical device claim, our team can help you understand the legal considerations involved.
If you or a loved one experienced a serious injury following surgery involving a surgical stapler or implantable staples, you may have questions about your legal options.
Goza & Honnold has experience handling complex medical device litigation and can discuss whether your circumstances warrant further legal evaluation.
Call (913) 451-3433 or contact Goza & Honnold online to schedule a consultation.
Goza & Honnold, LLC 9500 Nall Avenue, Suite 400 Overland Park, KS 66207
The availability and value of any legal claim depend on the individual facts, medical evidence, applicable law, filing deadlines, and other circumstances. Past results do not guarantee future outcomes.
If you or a loved one has been hurt, you don't have to face the legal process alone. Our attorneys are ready to listen, answer your questions, and help you understand your legal options.
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