FDA recall Z-1553-2020

Insulet Corporation · Class II · device

Product

Omnipod DASH Personal Diabetes Manager (PDM), Catalog numbers US: 18239 M/D: PDM-USA1-D001-MG-USA1 EU: PT-000010 - M/D: INT1-D001-MG PT-000011 M/D: INT1-D001-MM UDI 10385082000009 The Omnipod DASH Personal Diabetes Manager (PDM) is a mobile, handheld Android device that is intended to communicate with the Omnipod DASH Pod (pump).

Reason for recall

In certain scenarios, the Omnipod DASH PDM may suggest an inaccurate bolus amount based on a blood glucose value that is more than 10 minutes old when the user does not exit the bolus calculator as designed or when a system alarm interrupts a bolus calculation. If the user delivers the bolus, this may lead to hypoglycemia or hyperglycemia.

Distribution

US Nationwide distribution. Foreign distribution to Italy, Netherlands, and United Kingdom.

Key facts

Status
Terminated
Initiation date
2020-02-13
Report date
2020-04-01
Termination date
2021-09-14
Voluntary/Mandated
Voluntary: Firm initiated
Location
Acton, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1553-2020