Recall archive / FDA device enforcement
Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit. — FDA record Z-1370-2026
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Dec 31, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit.
- Reason
- 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.
- Classification
- Class II
- Recalling firm
- Medica Corporation
- Quantity
- 1,578 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1370-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Model No. 7303, UDI-DI: 00840095607575, Lot No. 25XXX. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
International distribution to the countries of Russia, Bulgaria, Kazakhstan, Ukraine, Pakistan, Belarus.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Feb 25, 2026
- Recall initiation date
- Dec 31, 2025
- Center classification date
- Feb 13, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.