Class II

Medical Device Recall: VariSoft Infusion Set, Single Use.

Unomedical A/S · July 23, 2024

Reason for Recall

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

Distribution

US Nationwide distribution in the state of California.

States Affected

NATIONWIDE

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3186-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.