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Medtronic announces voluntary recall of diabetes infusion sets


Medtronic plc has started to inform patients worldwide of a voluntary recall of specific lots of infusion sets used with all models of Medtronic insulin pumps.

By Team ABLE

Medtronic plc has started to inform patients worldwide of a voluntary recall of specific lots of infusion sets used with all models of Medtronic insulin pumps.

The recall is related to a certain discontinued component in these infusion sets and does not include insulin pumps or glucose sensors.

The company determined, through recent field reports from patients and root cause analysis, that a component, the vent membrane, in the recalled infusion sets may be susceptible to being blocked by fluid during the process of priming/fill-tubing. This situation can lead to potential over-delivery of insulin shortly after an infusion set change, which may cause hypoglycemia.

Currently manufactured infusion sets, available to patients since April 2017, include a design update of this component which the company believes reduces the risk of insulin over-delivery after an infusion set change.
The company will work with patients to ensure recalled infusion sets with the discontinued component are returned and replaced with new infusion sets containing the updated component at no cost.

Medtronic has contacted the US Food and Drug Administration (FDA), along with other regulatory bodies around the world, to share information related to this issue. Medtronic has said it will continue working directly with government and regulatory authorities on this global voluntary recall.