A51

HealthCare Alerts

Class 2 Device Recall Steris
Class 2 Device Recall BehindtheEar hearing aids
Class 2 Device Recall IntheEar hearing aids
Class 2 Device Recall Bard Access Systems PowerPort isp M.R.I. Implantable Port
B. Braun Medical Inc. Issues Voluntary Nationwide Recall of Twenty-Two (22) Lots of Blood Administration Sets, Due to Potential for Leakage at the Joint Between the Blood Filters and Tubing
Class 2 Device Recall Atellica CH 930 Analyzer
Amneal Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Ranitidine Tablets, USP, 150mg and 300mg, and Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity
MiniMed™ 600 Series Pump Retainer Ring
Roche Diabetes Care Australia Pty Ltd — Accu-Chek Guide and Accu Chek Performa Blood Glucose Meters
Precision Dose Inc. Issues Voluntary Nationwide Recall of Ranitidine Oral Solution, USP 150 mg/10 mL Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity

Events