FDA recall Z-1996-2026

Beta Bionics, Inc. · Class II · device

Product

iLet Bionic Pancreas, REF: BB1001

Reason for recall

insulin pump software versions 1.4.2, and 1.4.3 issue with Dexcom Continuous Glucose Monitoring (CGM) G7 sensor may result in delayed CGM reading then switch to non-CGM dosing, leading to only basal/requested meal doses provided, no correction doses/insulin reductions/suspensions for high/low glucose unless blood glucose entered for sensor life or replacement. Potential health risks to users include severe hyperglycemia with and without DKA and severe hypoglycemia.

Distribution

US Nationwide distribution in the states of TX, PA, AL, MI, OH, FL, TN, GA.

Key facts

Status
Ongoing
Initiation date
2026-03-12
Report date
2026-05-06
Voluntary/Mandated
Voluntary: Firm initiated
Location
Irvine, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1996-2026