FDAMarch 26, 2024device

Hillrom Welch Allyn Connex ProBP 3400 Digital Blood Pressure Device, marketed under the following models: a) PROBP 3400, SUREBP, BLUETOOTH, MOBILE,EU, Product Code 34BFST-2; b) PROBP 3400, SUREBP, BLUETOOTH, MOBILE,UK, Product Code 34BFST-4; c) PROBP 3400, SUREBP, BLUETOOTH, MOBILE,AU, Product Co...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Baxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical standards.

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

732094009385732094009378732094009361732094009248732094167733732094009231732094009057732094009040732094009033732094009026732094008852732094008845

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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