medical Class II Updated 2020-06-10

Insulet Corporation recalls Omnipod DASH Insulin Management System (mg/dL configuration)

Recalled Product

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.


Hazard / Issue

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.

Issued by

FDA

Distribution: The products were distributed to the following foreign countries: Italy, Netherlands, UK.
Lot/Code Info: UDI: PT - 000010 - 10385082000139; Lot Numbers: L000202
View official government recall

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →