medical MODERATE Updated 2026-05-06

Beta Bionics, Inc. recalls iLet Bionic Pancreas, REF: BB1001

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Recalled Product

iLet Bionic Pancreas, REF: BB1001

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Software versions 1.4.3, and 1.4.2

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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