Suntech Medical recalls Bravo Mini blood pressure monitors with model 250D due to battery misuse risks. Affected units may cause injury if rechargeable batteries are improperly handled.
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.
Suntech Medical is recalling Bravo Mini, Agilis Mini, and NBP One blood pressure monitors (model 250D) because improper use of rechargeable batteries could lead to injury. This recall affects devices sold with specific part numbers and serial numbers.
Improper use of rechargeable batteries in these monitors can cause injury. The hazard occurs when batteries are not handled correctly, potentially leading to electrical issues or damage to the device.
People who own or use the recalled blood pressure monitors are affected. Those who frequently handle the device's batteries or recharge them without proper precautions are at higher risk.
Check for the model 250D on the device. Look for part numbers: 99-0233-00 for Bravo Mini, NJ124 (99-0233-40) for Agilis Mini, or NBP One (99-0233-10). All units have serial numbers.
Ensure rechargeable batteries are used only as specified in the device manual to prevent injury.
Bravo Mini, Agilis Mini, and NBP One blood pressure monitors with model 250D.
Check for model 250D and part numbers: 99-0233-00 for Bravo Mini, NJ124 (99-0233-40) for Agilis Mini, or NBP One (99-0233-10). All units have serial numbers.
The recall does not specify a remedy, so check the manufacturer's website or contact them directly for guidance.
We’ve drafted a message you can send Suntech Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0810-2020 — Suntech Medical Suntech Medical Hello, I own a Suntech Medical that is covered by recall Z-0810-2020 from Suntech Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
