B-K Medical A/S recalls bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66.
An issue on the Dual Live Compare feature on the bkActiv system could result in a measurement error.
Read the official notice →- Date
- 2024-01-31
- Country
- United States
- Brand
- B-K Medical A/S
- Product
- bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66.
- Classification
- Class II
- Units
- US Nationwide distribution including in the states of AL, AZ, CA, FL, GA, ID,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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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