InfuTronix recalls

InfuTronix has 4 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 3 Apr 2024. 3 are still ongoing. The most frequent reason is packaging defects.

Total recalls4since 2019

Last 12 months0reported

Class I250% of total

Ongoing3latest 3 Apr 2024

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 2 50%Class II 2 50%Class III 0 0%

Why infutronix is recalled

Packaging Defects375%
Device Malfunction125%

Product types

Infusion Pumps375%
Heart & Vascular Devices125%

By year

2024250%
2022125%
2019125%

Ongoing infutronix recalls

3 active

Reported	Class	Recall	Company	Reason	Where
3 Apr 2024Device	CLASS I	Nimbus II Infusion System recalled by InfuTronix	InfuTronix	Packaging Defects	Nationwide
3 Apr 2024Device	CLASS I	Nimbus Administration Set recalled by InfuTronix	InfuTronix	Packaging Defects	Nationwide
6 Apr 2022Device	CLASS II	Nimbus PainPro Ambulatory Infusion Pumps recalled by InfuTronix	InfuTronix	Device Malfunction	Nationwide

All infutronix recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
3 Apr 2024Device	CLASS I	Nimbus II Infusion System recalled by InfuTronix	InfuTronix	Packaging Defects	Nationwide
3 Apr 2024Device	CLASS I	Nimbus Administration Set recalled by InfuTronix	InfuTronix	Packaging Defects	Nationwide
6 Apr 2022Device	CLASS II	Nimbus PainPro Ambulatory Infusion Pumps recalled by InfuTronix	InfuTronix	Device Malfunction	Nationwide
31 Jul 2019Device	CLASS II	Nimbus Administration Set recalled by InfuTronix	InfuTronix	Packaging Defects	MA

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.