Tag: medical_device_recalls

FDA Updates BD Alaris Infusion Set Recall, Warns of Worse Pump Performance

5 Oct 2026 4:44 p.m. · Source: US Food and Drug Administration

BD and CareFusion issue an updated letter warning that some BD Alaris Pump Infusion Sets perform worse than previously disclosed, with deviations at low rates and bolus volumes.

Health Business Science & Technology USA Medical Science Law Enforcement Federal Government Product Recall BD Alaris Pump Infusion Sets CareFusion 303 BD Alaris Pump Module 8100 US Food and Drug Administration Medical Device Recalls Guardrails Suite MX Food Recalls FDA Drugs
FDA: ICU Medical Drops Enhanced Inspection Advice for IV Tubing Sets After Discoloration Probe

5 Oct 2026 4:42 p.m. · Source: US Food and Drug Administration

ICU Medical has ended its recommended enhanced inspections of certain IV tubing sets after finding black specks and discoloration in drip chambers are intrinsic to the PVC material and pose no patient risk.

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