J&J Echelon Flex Endopath Staplers Lawsuit Investigation

Sauder Schlekopf is investigating litigation related to Johnson & Johnson recalled Echelon Flex Endopath staplers, distributed in August and September in the United States.

As reported by Bloomberg on Oct. 31, 2019:

Johnson & Johnson is recalling a surgical stapler after reports that seven patients were seriously injured and one died, the U.S. Food and Drug Administration said Thursday.

The device, made by J&J’s Ethicon unit, is used to simultaneously cut and staple tissue back together during surgery. But problems with a part caused misformed staples that failed to properly close incisions, the FDA said in a statement, leading to potential leakage, bleeding or more surgery.

The FDA said it was a class I recall, the most serious category declared only when there is a risk of serious harm or death. The FDA didn’t say whether the injuries and the death were directly caused by the stapler malfunctioning.

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Sauder Schelkopf is a nationally recognized class action and personal injury law firm. The firm’s partners currently serve as court appointed lead counsel in courts across the country and have been selected by the National Trial Lawyers Association as some of the Top 100 Trial Lawyers in Pennsylvania since 2012. The attorneys at Sauder Schelkopf have recovered over $500 million on behalf of their clients and class members.

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