Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Model 250D Ambulatory Blood Pressure Monitor labeled under the following Recalled by Suntech Medical, Inc. Due to The Bravo Mini (Model 250D), Agilis Mini (Model...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Suntech Medical, Inc. directly.
Affected Products
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).
Quantity: 384 units
Why Was This Recalled?
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.
Where Was This Sold?
No US Distribution; Internationally distributed to France, S. America
About Suntech Medical, Inc.
Suntech Medical, Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report