FDA recall Z-1544-2024

Unomedical A/S · Class II · device

Product

Neria Soft Infusion Set, Product Code 507302, intravascular administration set

Reason for recall

Specific lots of Neria Soft Infusion Sets, which have been shipped into the US Market, have been shipped with the incorrect Instruction for Use (IFU) within the final pack. The IFU included is the IFU registered for the Rest of World (ROW) countries. The difference between the US IFU and the ROW IFU is the addition of an intended use section in the ROW IFU.

Distribution

US Nationwide distribution in the state of Florida.

Key facts

Status
Ongoing
Initiation date
2024-03-05
Report date
2024-04-24
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lejre, Denmark

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1544-2024