Recall
FDAHealthAugust 13, 2025

Beta Bionics, Inc. — iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software

⚠️ it was found that in versions 1.3.7, 1.4.2, and 1.4.3, the Lock Screen and Limited Access Passcode Screen on the iLet graphical user interface (GUI) include certain icons displayed in the status bar that are active, thereby allowing the user to bypass those screens when those icons on the status bar are pressed, allowing unauthorized access while the device is in Limited Access Mode. A Health Risk associated with Limited access mode includes severe hypoglycemia due to unauthorized access to the iLet if someone were to make unauthorized meal announcements or stopped insulin delivery.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
August 13, 2025

US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, LA, MA, MD, ME, MI, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WY AND WASHINGTON DC.

What's affected?

Product
iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software
Lot code
ILet Ace Pumps containing software version BOM000036 Rev C (version 1.4.2) or older.

Additional details

ILet Ace Pumps containing software version BOM000036 Rev C (version 1.4.2) or older.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 15 units.

View original FDA notice →

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