Reported Jan 22, 2020 · Terminated
Model 250D Ambulatory Blood Pressure Monitor labeled under the following brands: Bravo Mini, part number 99-0233-00;…
Suntech Medical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Suntech Medical, Inc. · 507 Airport Blvd Ste 117 · Morrisville, NC · 27560-8200
Is this the product you have?
- Model 250D Ambulatory Blood Pressure Monitor
- labeled under the following brandsBravo Mini, part number 99-0233-00; Agilis Mini, part number NJ124 (99-0233-40); and NBP One, part number NBP One (99-0233-10)
- Lot codes and dates
- All serial numbers.
- Amount recalled
- 384 units
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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