FDA recall Z-0591-2024

Insulet Corporation · Class I · device

Product

Omnipod 5 App (on compatible Android smartphones), Software Versions 1.1 - 1.2.3 (current). US: PT-000599- Omnipod 5 App Software Package (provided through Google Play), EU: PT-001323- Omnipod 5 App Software Package (provided on locked-down Controllers (PT-001194 and PT-001193). Used to control an insulin pump.

Reason for recall

The bolus calculator is not recording the decimal point if it is the first value entered when changing a bolus dose. This may lead to an over-delivery of insulin to the user if the user does not recognize the error on the bolus calculator screen or the confirmation screen prior to starting the bolus.

Distribution

Worldwide distribution - US Nationwide and the countries of Germany and UK.

Key facts

Status
Ongoing
Initiation date
2023-11-30
Report date
2024-01-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
Acton, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0591-2024