A51

HealthCare Alerts

BD Announces Voluntary Recall of ChloraPrep™ 3 mL Applicator in Specific U.S. Territories and Countries
FDA updates on hand sanitizers consumers should not use
CME America Updates Recall of BodyGuard Infusion Pump System Due to Risk of Over-, and Under-infusion
Class 4 Medicines Defect Information: Crescent Pharma Ltd, SyreniRing 0.120 mg/0.015 mg per 24 hours, vaginal delivery system, EL (20)A/36
ICS Medical Advisory (ICSMA-20-212-01) Philips DreamMapper
Maquiladora Miniara S.A. de C.V. Issues Voluntary Nationwide Recall of Shine and Clean Hand Sanitizer and Due to Potential Presence of Undeclared Methanol (Wood Alcohol)
Philips sterilizable defibrillator internal paddles (specific models) – may fail to deliver therapy if pre-use checks are not followed
Alert (AA20-205A) NSA and CISA Recommend Immediate Actions to Reduce Exposure Across Operational Technologies and Control Systems
Fresenius Kabi Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine
ICS Medical Advisory (ICSMA-20-170-02) Baxter PrismaFlex and PrisMax (Update B)

Events