Ethicon Surgical Stapler Recall

Ethicon surgical stapler

The recent recall of the Ethicon surgical stapler raised concerns about its quality and safety. The FDA closely monitors the safety of these devices, and they received hundreds of reports of deaths and malfunctions from users. Read on to learn about the safety issues related to the Ethicon stapler. And if you want to avoid these issues, read on! Here are some important facts about this recalled surgical stapler. Hopefully, you’ll be safer using this device.

Malformed staples

An FDA recall has been issued for an Ethicon(r) Surgical Stapler due to potentially malformed staples. The product has caused several serious injuries, including hemorrhaging and shock. The recalled products were used in over 92,000 surgeries. This recall involves 92,496 staplers manufactured between March 6th, 2018, and March 8th, 2019. The recall stems from a manufacturing process shift, which led to uncut stapler washers that resulted in insufficient firing surgical staples lawsuit and malformed staples.


In a recent recall, the Food and Drug Administration (FDA) warned medical professionals of a possible risk of a stapler that leaks. This recall applies to the Ethicon Endo Curved Intraluminal Stapler, product codes CDH21A and CDH25A. In addition to a risk of colorectal cancer, these staplers may cause serious injuries and even death.


If you or a loved one have suffered from bleeding from an Ethicon surgical stapler, you may be eligible to file a lawsuit. The FDA has issued an open letter to health care providers, warning them of the dangers of these devices. The agency received over 41,000 reports of adverse events related to surgical staplers. These reports included 9,000 cases of serious injury, including 366 deaths.

Complications after surgery

The FDA has recalled Ethicon’s Endo Curved Intraluminal Stapler. The device contains a defective component that can cause malformed staples in patients. It has been linked to colorectal cancer. If you are planning to use an Ethicon surgical stapler, you should ask your surgeon if it is recalled. Fortunately, the company has issued a product recall for all affected staplers.

Legal action

The Ethicon surgical stapler has been the source of thousands of lawsuits filed in the United States by medical patients who were injured by the defective device. Many patients have reported tissue damage, infection, and death, and a surgical stapler lawyer can help you seek compensation for your losses. In some cases, the stapler was so defective that it was ejected from the body, causing serious injury to the patient.

Johnson & Johnson

In a recent lawsuit, a plaintiff suffered severe injuries caused by a defective Johnson & Johnson Ethicon surgical stapler. He sued Johnson & Johnson and its subsidiary, Ethicon, for failing to manufacture and market a stapler free of defects. His attorney, Panish, Kaufman, and Sonstein, of Panish, Shea, Boyle, & Ravipudi LLP, is representing him.


The Ethicon surgical stapler has been recalled by the U.S. Food and Drug Administration after several reports of malformed staples. These staples can cause significant tissue damage, resulting in prolonged surgery and additional surgeries. Malformed staples may also lead to bleeding, anastomotic leak, or hemorrhagic shock. These complications can be life-threatening, and the recall could affect thousands of people.