Johnson and Johnson has recalled over 157,000 surgical stapler devices and accessories used in hemorrhoid correction procedures. The recall came after the U. S. Food and Drug Administration assigned a Class 1, it’s most serious classification, to the devices and said that use of the staplers could cause serious injuries and even death. According to the FDA, the Johnson and Johnson staplers were recalled because they could malfunction or misfire during a procedure, causing incomplete staple formation. Patients may suffer complications from the use of these stapler devices resulting in:
Severe pain and bleeding
Rectal wall damage
Johnson and Johnson Ethicon Stapler Products Recalled
Transtar Circular Stapler Procedure Set
Proximate HCS Hemorrhoidal Circular Stapler and Accessories
Proximate PPH Hemorrhoidal Circular Stapler and Accessories
These products were manufactured and distributed between April 2011 and July 2012.
The attorneys at the Law Offices of Henry Hanflik are leaders in unsafe products and medical device litigation. Our experienced attorneys and staff have the knowledge and resources to effectively and efficiently represent you. If you or your loved one have been injured by a Johnson and Johnson surgical stapler device, call our office now for a free consultation at 810-720-4000 or 888- 905-4632.