Model 250D Blood Pressure Monitor (Suntech) – battery safety (2019)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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).
Brand
Suntech Medical, Inc.
Lot Codes / Batch Numbers
All serial numbers.
Products Sold
All serial numbers.
Suntech Medical, Inc. is recalling Model 250D Ambulatory Blood Pressure Monitor labeled under the following brands: Bravo Mini, part n due to 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 ba. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consignees notified via email with recall letter dated 12/11/2019. The letter identified affected product, stated reason for recall, and requested product not to be used, and to be returned to the distributor. A Recall Acknowledgement Form was requested to be returned by e-mail.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026