Inari Medical - Oak Canyon recalls Artix MT Thrombectomy Device, REF: 32-102
Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery,…
Read the official notice →- Date
- 2025-05-14
- Country
- United States
- Brand
- Inari Medical - Oak Canyon
- Product
- Artix MT Thrombectomy Device, REF: 32-102
- Classification
- Class II
- Units
- US Nationwide distribution in the states of FL, IL, WI, KY, TX, CA, OH, GA,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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