Recall and safety-notice records

Records aggregated from the official sources MedWatcher monitors. Each record links back to its source with the agency identifier and dates. Sample records are labeled.

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Recall and safety-notice records

Records aggregated from the official sources MedWatcher monitors. Each record links back to its source with the agency identifier and dates. Sample records are labeled.

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BD Alaris Infusion System recall — FDA event 97067

Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.

FDA · FDA event 97067Posted Aug 6, 2025BD Alaris Infusion System

Class I recallOngoing

Plum Duo Infusion System, List Number: 400020401 recall — FDA event 97186

ICU Medical identified two sequences of programming events and alarm interactions that may cause the user interface to become unresponsive.

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BD Alaris Infusion System recall — FDA event 97067

FDA · FDA event 97067Posted Aug 6, 2025BD Alaris Infusion System

Class I recallOngoing

Plum Duo Infusion System, List Number: 400020401 recall — FDA event 97186

ICU Medical identified two sequences of programming events and alarm interactions that may cause the user interface to become unresponsive.

Recall and safety-notice records

Recall and safety-notice records

Filters

Filters

BD Alaris Infusion System recall — FDA event 97067

Plum Duo Infusion System, List Number: 400020401 recall — FDA event 97186

Filters

Filters

BD Alaris Infusion System recall — FDA event 97067

Plum Duo Infusion System, List Number: 400020401 recall — FDA event 97186

Baxter SIGMA Spectrum Infusion Pump V6 and V8 recall — FDA event 97072

BiPAP A40 Ventilator recall — FDA event 96948

Servo-n Ventilator System recall — FDA event 97032

Omnipod 5 Automated Insulin Delivery System recall — FDA event 96945

Dexcom G6 and G7 receiver recall: missed audible glucose alerts

Newport HT70 Ventilator recall — FDA event 96774