FDA Issues Class I Recall For Ethicon’s Circular Surgical Staplers

KBD previously noted problems with surgical staplers. Once again, defective surgical staplers are in the news. Following the FDA’s March 2019 warnings to surgeons about...

Public Access to Medical Device Problem Files – FDA Says

FDA says secret files on medical device problems will be opened to the public One of the ways that consumers should be able to stay...

After Injuries, FDA Orders Transvaginal Mesh Off The Market

Lawsuits against manufacturers of surgical mesh to treat pelvic organ prolapse have been filed in the tens of thousands after the first reports of possible...

Medical Scopes Still Causing Superbug Infections And Deaths

Medical Scopes Still Causing Superbug Infections And Deaths During an endoscopy, medical scopes are inserted into a patient's body. Whenever a foreign instrument is placed...

FDA Orders Manufacturers to Stop Selling Transvaginal Mesh

April 16, 2019, the United States Food and Drug Administration (FDA) published a press release that indicated it had officially and directly ordered all known...

Hernia Mesh Symptoms

Hernia Mesh Symptoms There are numerous health complications associated with defective hernia mesh implants that people should watch out for as some of these cause...

Surgical Staplers & Staples Found Unsafe

Recent reports of defective surgical staplers and staples have patients, doctors, and the U.S. Food and Drug Administration (FDA) concerned. What Are Surgical Staplers? Surgical...

FDA Warns Breast Implant Manufacturers

Two breast implant manufacturers were recently issued warning letters from the U.S. Food and Drug Administration (FDA) because they did not comply with the requirements...

Lime Scooter Defects Cause Injuries

Lime, a scooter-based ride-sharing app, has recently run into trouble with their software and hardware which has been making their scooters malfunction and cause injuries...

Robotically-Assisted Surgical Devices and Women’s Health

Safety communication has recently been issued by the Food and Drug Administration (FDA) involving the effectiveness and safety of cancer procedures utilizing robotically-assisted surgical devices....

Defective Devices

FDA Issues Class I Recall For Ethicon’s Circular Surgical Staplers

Public Access to Medical Device Problem Files – FDA Says

After Injuries, FDA Orders Transvaginal Mesh Off The Market

Medical Scopes Still Causing Superbug Infections And Deaths

FDA Orders Manufacturers to Stop Selling Transvaginal Mesh

Hernia Mesh Symptoms

Surgical Staplers & Staples Found Unsafe

FDA Warns Breast Implant Manufacturers

Lime Scooter Defects Cause Injuries

Robotically-Assisted Surgical Devices and Women’s Health

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