Tandem Diabetes Care, Inc.: Device Recall

Recall #Z-1519-2025 · 02/27/2025

Class I: Dangerous

Recall Details

Recall Number
Z-1519-2025
Classification
Class I
Product Type
Device
Recalling Firm
Tandem Diabetes Care, Inc.
Status
Ongoing
Date Initiated
02/27/2025
Location
San Diego, CA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
63 units

Reason for Recall

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.

Product Description

t:slim X2 Insulin Pump with Interoperable Technology

Distribution Pattern

US: AZ, CA, CO, CT, FL, HI, IA, ID, IL, IN, MD, ME, MI, MO, MS, NC, ND, NE, NJ, NM, NV, NY, OH, PA, TX, UT, VA, WA, WI OUS: N/A

Other Recalls by Tandem Diabetes Care, Inc.

View all recalls by Tandem Diabetes Care, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.