Welch Allyn recalls ProBP 3400 blood pressure devices with model 34XFHT-B due to potential fluid ingress causing electrical short and shock risk. Affected units include handheld, desk, and wall mount models.
Potential Risk of fluid ingress to the power supplies, resulting in risk of an internal electrical short and possible electrical shock
Welch Allyn is recalling ProBP 3400 blood pressure devices (model 34XFHT-B) because water or other fluids could enter the device and cause electrical shorts, potentially leading to shock. This affects handheld, desk, and wall-mounted models.
Fluids entering the device's power supply could cause an internal electrical short. This might lead to electrical shock if the device is used while wet or in humid conditions.
People who own or use the ProBP 3400 blood pressure device with model 34XFHT-B are affected. Those who use the device in wet environments or near water sources are at higher risk.
Check for the model number 34XFHT-B on the device. The ProBP 3400 includes handheld, desk mount, and wall mount versions. All units with this model number are affected.
Inspect the device for signs of water exposure or moisture, especially if used near water sources.
Reach out to Welch Allyn directly for guidance on next steps if you have the affected model.
The recall states that fluid ingress could cause electrical shorts, so even dry devices might be at risk if they could become wet.
Check for the model number 34XFHT-B on the device. The ProBP 3400 includes handheld, desk mount, and wall mount versions.
The recall does not specify a remedy, so contact Welch Allyn directly for guidance.
We’ve drafted a message you can send Welch Allyn to request your refund or repair — edit it as you like.
Subject: Recall Z-1673-2021 — Welch Allyn Welch Allyn Hello, I own a Welch Allyn that is covered by recall Z-1673-2021 from Welch Allyn. 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.
