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Woman's Bowel Stapled Shut by Doctor Wielding Defective Staple Gun
  • USA - English


News provided by

Alexander Law Group , LLP

Jul 31, 2013, 17:20 ET

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San Jose, California (PRWEB) July 31, 2013 -- Retired San Jose Police Officer Florence Kuhlmann, 59, had her bowel stapled shut by a surgeon using a defective staple gun, according to a complaint filed by the Alexander Law Group.

The complaint alleges defendants Johnson & Johnson, the Pleasanton Surgery Center, LLC and Rakhee N. Shah, M.D. of Pleasanton as the parties responsible for the devastating injuries that occurred on January 27, 2012 during hemorrhoid surgery at the Pleasanton Surgery Center.

Florence has suffered unbelievably, starting with 21 days of emergency hospitalization, massive infection and major abdominal surgeries...

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The complaint filed in Alameda County [Superior Court of California, County of Alameda; Case Number: RG 13675753] states the staple gun was manufactured by Ethicon Endo-Surgery, LLC, a subsidiary of Johnson & Johnson.

“In the hands of Dr. Shah this staple gun caused lifetime injuries to Florence Kuhlmann," said attorney Richard Alexander.

The staple gun, labelled a Proximate PPH Procedure Set PPHO3 by Ethicon Endo, was recalled on August 3, 2012, six months after Florence Kuhlmann’s surgery.
(FDA; http://www.fda.gov/medicaldevices/safety/listofrecalls/ucm325570.htm)

The complaint alleges the manufacturer knew the dangers of the product, including, “misfiring, incomplete firing strokes, and incomplete staple formation and the resulting consequences for many patients included sphincter dysfunction, rectal wall damage, sepsis, and bleeding.”

"Florence has suffered unbelievably, starting with 21 days of emergency hospitalization, massive infection and major abdominal surgeries that resulted in a full laparotomy -- surgical opening of her complete abdomen -- and a colostomy,” Alexander said. "She is plagued by external and internal scarring, continues to struggle with a deformed bowel, has been forced to wear a colostomy bag and has had multiple medical procedures attempting to restore her damaged bowel.”

“A search of the FDA Manufacturer and User Device Experience internet database* reveals more than 750 adverse events, two deaths and over 150 serious injuries referencing this product. Between March, 2007 and June, 2012 there were nearly 100 cases involving injuries related to the firing of Ehticon-Endo’s staple gun during an operation,” said Alexander. “We believe this is the tip of the iceberg,” he added.

"This staple gun should have been recalled long before Florence’s surgery,” said Alexander. “Florence Kuhlmann’s life has been changed forever.”

  • Link to FDA website to search on this site, enter PPH for brand name and ethicon for manufacturer. Select 1/1/2000 to present

Rich Robinson, Alexander Law Group , LLP, http://www.alexanderinjury.com/, 408 289-1776, [email protected]

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