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Suntech Medical, Inc. recalls Model 250D Ambulatory Blood Pressure Monitor labeled under the following brands: Bravo Mini, part number 99-0233-00; Ag
Recalled January 22, 2020 · FDA recall Z-0810-2020 · Suntech Medical
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. · FDA Class II
Units
384 units
Sold at
No US Distribution; Internationally distributed to France, S. America
Description
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.
Product
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).
Manufacturer(s)
Suntech Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →