Suntech Medical, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0810-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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).

Product Classification:

Class II

Date Initiated: December 11, 2019

Date Posted: January 22, 2020

Recall Number: Z-0810-2020

Event ID: 84531

Reason for Recall:

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.

Status: Terminated

Product Quantity: 384 units

Code Information:

All serial numbers.

Distribution Pattern:

No US Distribution; Internationally distributed to France, S. America

Voluntary or Mandated:

Voluntary: Firm initiated