Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ProBP 3400 Digital Blood Pressure Device ((handheld Recalled by Welch Allyn Inc Due to Potential Risk of fluid ingress to the power...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Welch Allyn Inc directly.
Affected Products
ProBP 3400 Digital Blood Pressure Device ((handheld, desk mount, wall mount models) Model: 34XFHT-B Intended: ProBP 3400 automatically measures systolic and diastolic pressure (excluding neonates) and pulse rate, as well as calculates Mean Arterial Pressure (MAP).
Quantity: 119770 units
Why Was This Recalled?
Potential Risk of fluid ingress to the power supplies, resulting in risk of an internal electrical short and possible electrical shock
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Welch Allyn Inc
Welch Allyn Inc has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report