Class II

Medical Device Recall: Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit.

Medica Corporation · December 31, 2025

Reason for Recall

A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica s capillary tubes.

Distribution

International distribution to the countries of Russia, Bulgaria, Kazakhstan, Ukraine, Pakistan, Belarus.

Quantity Affected

1,578 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1370-2026

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.