Stryker, Inc. recalls Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
Read the official notice →- Date
- 2024-02-21
- Country
- United States
- Brand
- Stryker
- Product
- Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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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