Medica Corporation: Medical Device Recall in 2026 - (Recall #: Z-1370-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit.

Product Classification:

Class II

Date Initiated: December 31, 2025

Date Posted: February 25, 2026

Recall Number: Z-1370-2026

Event ID: 98315

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.

Status: Ongoing

Product Quantity: 1,578 units

Code Information:

Model No. 7303, UDI-DI: 00840095607575, Lot No. 25XXX.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated