BLOG

Hidden FDA Database Concealed Reports of Surgical Stapler Malfunctions


fda

A hidden FDA database of medical device failures was shut down in June 2019. The database contains medical device reports submitted to the FDA via its Alternative Summary Reporting Program from 1999 to 2019. Reports which were sent to this database were not, until recently, made public. The Alternative Summary Reporting Program is a non-public database, unlike the FDA’s MAUDE database which publicly logs medical device failures or defects for public review.

surgical staplerThe Alternative Summary Reporting Program seems to have hidden a huge number of reports of malfunctions of surgical staplers. For example, in 2016 there were 84 reports of stapler malfunctions or injuries submitted to the FDA’s public MAUDE database, yet in that same year almost 10,000 reports of malfunctions were submitted via the Alternative Summary Reporting Program.

Growing Concern Over Surgical Stapler Malfunctions

 The FDA reports that over 56,000 reports of surgical stapler malfunctions were reported via the Alternative Summary Reporting Program between 2011 and 2018. Deaths must be reported via the MAUDE database, and over 400 surgical staple/stapler deaths were reported to the MAUDE database since 2011.

A 2013 study concluded that patients who have orthopedic surgery and have their wounds closed with surgical staplers face a higher risk of wound infections as compared to patients who had wounds closed with sutures.

A March 2019 FDA letter stated that 366 deaths and more than 9,000 serious injuries resulting from surgical staples and staplers were reported between January 2011 and March 2018.

Types Of Surgical Stapler Injuries:

  • Bleeding
  • Sepsis
  • Internal tissue tears
  • Fistula formation
  • Organ tears
  • Death

Ethicon Recalls Surgical Staplers

Ethicon, a subsidiary of Johnson & Johnson, manufactures the Endo-Surgery Curved Intraluminlal Stapler and the Endo-Surgery Endoscopic Curved Intraluminal Stapler. Ethicon recalled 92,496 of these devices in April 2019.  Surgical staplers are commonly used in gastrointestinal tract surgeries.

Surgical Stapler Injury Lawsuit

Nadrich & Cohen and its legal teams are currently representing surgical stapler patients who were injured due to a defective surgical stapler which caused one of the above injuries. The lawyers at Nadrich & Cohen offer a 100% free and confidential surgical stapler case evaluation. If you or a loved one has suffered a surgical stapler injury, immediately contact our office at 1-800-718-4658 for a free consultation.

Learn More...


August 29, 2018

Types of Burn Injuries

Over the years, our law firm has been greatly impacted by burn victim stories. ...


November 6, 2018

What If The Police Report Says The Accident Is My Fault

We have obtained financial settlements for clients even when there is at first a...


January 30, 2019

2018 California Wildfire Costs To Exceed $9 Billion

On November 8, 2018, two fires ravaged California. The Camp Fire, the deadliest...

Do I Have A Case?

We offer free consultation. No office visit required, we will get back to you within 24 hours.

  • This field is for validation purposes and should be left unchanged.

 

What can we do for you?

  • Answer your legal question.
  • Provide a Free Case Evaluation.
  • Schedule an appointment.

 

Why
Choose Us?

  • Available 24/7
  • Trusted Since 1990
  • Local to You
  • Recovered $350,000,000
  • 5 Star Reviews
  • Free Case Evaluation
  • VIP Service
  • No Win, No Fee

Latest Law Post


October 15, 2019

Zantac Recalled In All Markets

GlaxoSmithKline said on October 8, 2019 that it was recalling their popular heartburn medication Zantac in all markets as a precaution. This comes mere days after the U.S. Food and Drug Administration (FDA) found “unacceptable” levels of the carcinogen NDMA in the medicine.


October 2, 2019

Hidden FDA Database Concealed Reports of Surgical Stapler Malfunctions

A hidden FDA database of medical device failures was shut down in June 2019. The database contains medical device reports submitted to the FDA via its Alternative Summary Reporting Program from 1999 to 2019. Reports which were sent to this database were not, until recently, made public. The Alternative Summary Reporting Program is a non-public database, unlike the FDA’s MAUDE database which publicly logs medical device failures or defects for public review.

 

We are Personal Injury Lawyers representing accident victims throughout California.
For 30 years, the law firm of Nadrich & Cohen, LLP has helped injury victims
obtain the compensation they deserve.