FDA Recalls, Food, Drug & Medical Device Alerts - Page 11 of 27

Latest food, drug, and medical device recalls issued by the U.S. Food and Drug Administration. Class I, II, and III recall classifications, affected products, and consumer guidance.

Recall of Diversatek Healthcare Viper 3-Stage Wire Guided Balloon Dilator

FDA Mandated Recall of Uvlizer Handheld UV-C Germicidal Wand

Recall of OER-ELITE Endoscope Reprocessor Connecting Tubes

FDA Recall of LSL Healthcare Infant Central Line Dressing Change Kit

Medline Control Syringes Recall Over Rescinded Regulatory Clearances

Recall of Olympus Thunderbeat II Shears Due to Detachment Risk

FDA Recall of Olympus OER-ELITE Endoscope Reprocessor Connecting Tubes

FDA Recall of Medline Convenience Kits Due to Unapproved Design Changes

Medline Syringe Kits Recall for Unapproved Design Changes

Recall of Medline GYN Laparoscopy Pack

FDA Recalls Medline Syringes Due to Regulatory Issues

Medline Industries LP Recall of Medical Devices

FDA Recalls Medline Medical Kits Due to Regulatory Issues

FDA Recall of Olympus Thunderbeat II Shears for Potential Detachment

FDA Recall of Medline ARTHROSCOPY PACK Due to Regulatory Clearance Issues

FDA Recall of Angiodynamics Soft-Vu Angiographic Catheter Due to Manufacturing Defect

FDA Recall of Arrowg+ard Blue Plus Four-Lumen CVC Kits

Recall of LSL Healthcare IV Start Kit

FDA Recall of AccuVu Angiographic Catheter Due to Manufacturing Defect

FDA Recall of Avitene Ultrafoam Hemostat Due to Potential Contamination

FDA Recall of Flamingo Funnel Medium by SurgiSmoke Solutions

Recall of LSL Healthcare Central Line Dressing Kit

Recall of Medline GENERAL LAPAROSCOPY Kits

Medline Industries Recalls Medical Devices Due to Regulatory Issues

Recall of LSL Healthcare Standard Central Line Dressing Change Kit

FDA Recall of Custom Convenience Kits Pre Op Kit - NS

Recall of Medline Convenience Kits Due to Design Changes

FDA Recall of OER-ELITE Endoscope Reprocessor Connecting Tubes

Recall of Medline DYNJ44813D Kits

FDA Recall of LeadCare Ultra Blood Lead Test Kit

Recall of Percutaneous Sheath Introducer by Arrow International

Recall of Soft-Vu Angiographic Catheter Due to Manufacturing Defect

FDA Recall of FLEXTIP PLUS Epidural Catheter Announced

FDA Recall of Soft-Vu Angiographic Catheter by Angiodynamics

FDA Recall of FoundationOneCDx Software by Foundation Medicine

Medline Convenience Kits Recall for Unapproved Design Changes

Recall of Soft-Vu Angiographic Catheter by Angiodynamics, Inc.

Recall of Medline Breast Pack Kits Due to Regulatory Clearance Issues

Medline Namic Syringes Recall Over Regulatory Issues

Recall of ARROW Pressure Injectable Central Venous Catheters

Recall of ARROW Radial Artery Catheterization Kits Due to Manufacturing Issue

FDA Issues Recall for Soft-Vu Angiographic Catheter Due to Manufacturing Defect

Recall of Access Total T4 Calibrator by Beckman Coulter Due to Accuracy Issues

FDA Recall of LeadCare II Blood Lead Test Kits

Medline Convenience Kits Recall Over Unapproved Design Changes

Recall of Rover Mobile X-ray System Due to Potential Malfunction

Medline Industries Recalls Medical Devices Over Regulatory Issues

Recall of Flamingo Funnel Small by SurgiSmoke Solutions

Medline Industries Recalls Medical Kits Over Regulatory Clearance Issues

Recall of Medline Hysteroscopy Pack and Sling Pack