Unomedical A/S: Medical Device Recall in 2024 - (Recall #: Z-3186-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

VariSoft Infusion Set, Single Use.

Product Classification:

Class II

Date Initiated: July 23, 2024

Date Posted: September 25, 2024

Recall Number: Z-3186-2024

Event ID: 95224

Reason for Recall:

Specific VariSoftTM Infusion Sets were packaged using incorrect secondary packaging (boxes) branded "Trusteel Infusion Set".

Status: Ongoing

Product Quantity:

Code Information:

UDI-DI: 05705244018747. Product Code: 1726035. Lot Number: 6005241

Distribution Pattern:

US Nationwide distribution in the state of California.

Voluntary or Mandated:

Voluntary: Firm initiated