Ethicon Surgical Stapler Recall

Ethicon Surgical Stapler Recall

The FDA recently announced the Ethicon Surgical Stapler Recall because it contains an out-of-spec component. Incorrectly placed staples can cause injury to patients or even death. The resulting staples may also lead to bleeding, anastomotic leak, hemorrhage, or even additional surgery. The resulting complications can cause a patient to undergo repeated surgeries, require additional surgeries, or even result in death.

If you or a loved one has been injured by an Ethicon surgical stapler, you may be able to file a product liability lawsuit against the company. Because this product is potentially dangerous, the company that manufactures it is responsible for any damages caused by faulty staplers. Patients and their families may also be able to recover monetary compensation. If you or a loved one has suffered from the faulty Ethicon Stapler Recall, contact a reputable law firm to discuss your options. A law firm with extensive experience handling defective medical devices may be able to help you make a successful case.

The FDA has issued a Class 1 Recall for Ethicon Surgical Staplers. This is the highest level of recall and means the product poses a high risk of causing serious injuries to patients. The recall affects 8.256 linear surgical staplers. If you have a stapler with a Class 1 recall, you should contact the manufacturer immediately to ensure your safety. You should avoid using this stapler until the company releases an updated recall notice.

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