FDAApril 2, 2020device

Omnipod DASH Insulin Management System (mg/dL configuration), Catalog Number PT000010 M/D: INT1D001MG - Product Usage: is intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

After the device has been in use for about 2 months, data processing in the PDM can be slowed such that the Bolus Calculator fails to accurately subtract the correct amout of IOB before suggesting a bolus amount.

What to do

FDA enforcement status: Terminated

Brands named

insulet

UPCs

10385082000139

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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