Medica Capillary Tubes recall (Medica Corporation)
Medical deviceClass IIOngoing
Summary: Medica Corporation is recalling 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.
What is being recalled
Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit.
Why
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.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
International distribution to the countries of Russia, Bulgaria, Kazakhstan, Ukraine, Pakistan, Belarus.
How to tell if yours is affected
Model No. 7303, UDI-DI: 00840095607575, Lot No. 25XXX.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1370-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | December 31, 2025 |
| Reported | February 25, 2026 |
| Company | Medica Corporation |
| Company location | Bedford, MA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 1,578 units |
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