FDAFebruary 27, 2025device

t:slim X2 Insulin Pump with Interoperable Technology

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is above 255 mg/dL at the start or end of a gap in data collection due to a lapse in connection from a paired continuous glucose monitor (CGM) sensor, which can lead to under-delivery or over-delivery of insulin based on inaccurate result leading to severe cases of hypoglycemia or hyperglycemia.

What to do

FDA enforcement status: Ongoing

Brands named

tandem diabetes caretandemtandem diabetes

UPCs

00389152407012

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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