Medica Capillary Tubes recall
Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit.
Why was Medica Capillary Tubes recalled?
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 should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model No. 7303, UDI-DI: 00840095607575, Lot No. 25XXX.
- Product
- Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit.
- Recalling firm
- Medica Corporation
- Quantity
- 1,578 units
- Distribution
- International distribution to the countries of Russia, Bulgaria, Kazakhstan, Ukraine, Pakistan, Belarus.
- Recall date
- February 25, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)