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 93106

Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.

FDA · FDA event 93106Posted Nov 7, 2023BD Alaris Infusion System

Class II recallOngoing

Omnipod 5 Automated Insulin Delivery System recall — FDA event 92909

An error message was received when using the Omnipod 5 App on compatible smartphones that prevented phone control users from controlling the Omnipod 5 Automated Insulin Delivery System from their Omnipod 5 App which may cause a delay in therapy. To reduce the…

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BD Alaris Infusion System recall — FDA event 93106

Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.

FDA · FDA event 93106Posted Nov 7, 2023BD Alaris Infusion System

Class II recallOngoing

Recall and safety-notice records

Recall and safety-notice records

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BD Alaris Infusion System recall — FDA event 93106

Omnipod 5 Automated Insulin Delivery System recall — FDA event 92909

Filters

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BD Alaris Infusion System recall — FDA event 93106

Omnipod 5 Automated Insulin Delivery System recall — FDA event 92909

ICU Medical Plum 360 Infusion System recall — FDA event 92630

FreeStyle Libre 2 Continuous Glucose Monitoring System recall — FDA event 92708