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Recall Observatory FDA recall evidence

Device product

iLet Bionic Pancreas, REF: BB1001

Z-2513-2026

September 23, 2025

Class II

Product summary

Firm
Beta Bionics, Inc.
Event
Event 98517
Status
Ongoing
Classification
Class II
Quantity
4580
Official record key
device-enforcement:Z-2513-2026

Official wording

Reason: The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfully slides the unlock slider on the Lock Screen, no screen transition occurs, and the user remains on the Lock Screen. Because the user cannot exit the Lock Screen, the user is unable to perform a cartridge change or meal announcement. If this occurs and therapy is in progress, therapy will continue normally until the insulin cartridge is depleted. The user will be unable to perform a cartridge change or a meal announcement and will be stuck on the screen until the battery fully drains. This can lead to hyperglycemia.

Code information: iLet ACE Pump firmware BOM000072 Rev C (version 3.3.6) and BOM000072 Rev B (version 3.3.4)

Distribution pattern: US: WI, HI, OH, ME, CO, NJ, NE, KY, SC, CA, TX, NH, NY, WA, PA, MD, FL, IA, GA, MI, VT, TN, IL, IN, KS, MA, LA, MS, NC, CT, MN, VA, OK, AR, AZ, MO, MT, RI, DC, NM, OR, ID, NV, AK, ND, DE, WV, WY, SD, UT, AL

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    firmware and all previous releases that a screen unlock failure