FDADecember 11, 2019device
Model 250D Ambulatory Blood Pressure Monitor labeled under the following brands: Bravo Mini, part number 99-0233-00; Agilis Mini, part number NJ124 (99-0233-40); and NBP One, part number NBP One (99-0233-10).
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The Bravo Mini (Model 250D), Agilis Mini (Model 250D), and NBP One (Model 250D) are being recalled because of a user safety issue when rechargeable batteries are misused in the product.
What to do
FDA enforcement status: Terminated
Brands named
suntech medicalsuntech
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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