Reported Jan 31, 2024 · Ongoing
bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66.
B-K Medical A/S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B-K Medical A/S · Mileparken 34 · Herlev, N/A · N/A
Is this the product you have?
bkActiv Ultrasound System 2300Model numbers 2300-56 and 2300-66
- Lot codes and dates
- All bkActive (2300-56 and 2300-66) Ultrasound systems, GTIN 05704916000264.
- Amount recalled
- N/A
Where it was sold
Why it was recalled
An issue on the Dual Live Compare feature on the bkActiv system could result in a measurement error.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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