Covidien Recalls Surgipro II Sutures Over Sterile Barrier Defects
FDA classifies recall of 135,875 suture units as Class II due to potential packaging tears that could lead to contamination and infection.
Recalls & Safety Alerts in North Haven, Connecticut
Every recalls & safety alerts report published for North Haven, Connecticut, newest first.
FDA Reports Ongoing Recall of Covidien V-Loc 90 Suture Devices
The FDA's enforcement report dated August 19, 2026, lists the Class II recall of V-Loc 90 Absorbable Wound Closure Devices as ongoing, citing a potential sterile barrier defect.
FDA Expands Covidien V-Loc 90 Suture Recall to Include Additional Sizes
The recall now covers 4-0, 3-0, 2-0, and 0 sizes in lengths from 15 to 45 centimeters, according to the FDA enforcement report.