Unetixs Vascular, Inc. recalls MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01
The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
Read the official notice →- Date
- 2023-03-08
- Country
- United States
- Brand
- Unetixs Vascular, Inc.
- Product
- MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and Global distribution.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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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