Access Now: AORN COVID-19 Clinical Support

Surgical Device Recalls

21-30 of 35

Ethicon Recalls Colorectal Staplers

Devices' difficult use created post-op complication risks.

Posted 10/30/12 | Post a comment

Stryker Recalling Unapproved Neptune Systems

FDA never cleared Neptune 1 Silver, Neptune 2 Ultra.

Posted 09/26/12 | Post a comment

Covidien's Surgical Stapler Recalled, Discontinued

Duet TRS's staples caused injuries after abdominal, thoracic surgeries.

Posted 08/24/12 | Post a comment

ASP Recalls Sterrad Biological Indicators

Product not effective through stated expiration date.

Posted 07/06/12 | Post a comment

FDA Updates Prep Product Recall

Contaminated povidone-iodine pads distributed under private labels, found in many kits.

Posted 09/30/11 | Post a comment

Group Urges FDA to Recall Surgical Mesh

Product exposes female patients to "serious risks," says Public Citizen.

Posted 08/25/11 | Post a comment

CDC Announces Propofol Recall

Two lots of Teva-manufactured propofol tested positive for high levels of endotoxin.

Posted 07/14/09 | Post a comment

AMO Voluntarily Recalls Healon D

Company says it has received "limited reports" of inflammatory reaction.

Posted 11/04/08 | Post a comment

advertiser banner