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" Pump Module model 8100 recall — FDA event 97871

Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital networks. This issue only affects the Interoperability workflow for devices with a DST invalid…

FDA · FDA event 97871Posted Jan 29, 2026

Class II recallOngoing

Baxter SIGMA Spectrum Infusion System recall — FDA event 98167

Certain pumps have potentially been released from service with defective grease applied to the cam and motor gears. Due to its low viscosity, the defective grease may lead to the device having insufficient lubrication on the cam, which could lead to premature…

Recall and safety-notice records

Recall and safety-notice records

Filters

Filters

BD Alaris" Pump Module model 8100 recall — FDA event 97871

Baxter SIGMA Spectrum Infusion System recall — FDA event 98167

Filters

Filters

BD Alaris" Pump Module model 8100 recall — FDA event 97871

Baxter SIGMA Spectrum Infusion System recall — FDA event 98167

ICU Medical Plum Duo Infusion Pump, List Numbers: 400020401 (US), recall — FDA event 98128

Plum Duo Infusion System, List Number 40002-04-01 recall — FDA event 98129

FreeStyle Libre 3 Continuous Glucose Monitoring System recall — FDA event 98049

Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005 recall — FDA event 98106

Ivenix Infusion System (IIS), LVP Software LVP-SW-0005 recall — FDA event 98009

Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, recall — FDA event 97971