Reported Apr 17, 2024 · Ongoing
Hillrom Welch Allyn Connex ProBP 3400 Digital Blood Pressure Device, marketed under the following models
Baxter Healthcare Corporation
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: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
Hillrom Welch Allyn Connex ProBP 3400 Digital Blood Pressure Device, marketed under the following models
23 of 23 products
| Model / number | Product as published |
|---|---|
34BFST-2 | PROBP 3400, SUREBP, BLUETOOTH, MOBILE,EU |
34BFST-4 | PROBP 3400, SUREBP, BLUETOOTH, MOBILE,UK |
34BFST-6 | PROBP 3400, SUREBP, BLUETOOTH, MOBILE,AU |
34BXST-2 | PROBP 3400, BLUETOOTH, MOBILE, EU |
34BXST-4 | PROBP 3400, BLUETOOTH, MOBILE, UK |
34BXST-7 | PROBP 3400, BLUETOOTH, MOBILE, ZA |
34XFST-2 | PROBP 3400, SUREBP, MOBILE, EU |
34XFST-4 | PROBP 3400, SUREBP, MOBILE, UK |
34XFST-6 | PROBP 3400, SUREBP, MOBILE, AU |
34XFST-7 | PROBP 3400, SUREBP, MOBILE, ZA |
34XXST-2 | PROBP 3400, MOBILE, EU |
34XXST-4 | PROBP 3400, MOBILE, UK |
34XXST-6 | PROBP 3400, MOBILE, AU |
34XXST-7 | PROBP 3400, MOBILE, ZA |
PWCD-5WT-2 | PROBP MOBILE STAND CORD ASSY EUROPE |
PWCD-5WT-4 | PROBP MOBILE STAND CORD ASSY UK |
PWCD-5WT-6 | PROBP MOBILE STAND CORD ASSY AUST |
| — | PROBP MOBILE STAND CORD ASSY |
PWCD-5WT-7 | AFRICA |
PWCD-6WT-2 | PROBP MOBILE STAND CORD ASSY EUROPE |
- Lot codes and dates
21 of 21 products
Products covered by this recall # Barcodes Product as published 1 73209400938534BFST-2, UDI/DI 732094009385 2 73209400937834BFST-4, UDI/DI 732094009378 3 73209400936134BFST-6, UDI/DI 732094009361 4 73209400924834BXST-2, UDI/DI 732094009248 5 73209416773334BXST-4, UDI/DI 732094167733 6 73209400923134BXST-7, UDI/DI 732094009231 7 73209400905734XFST-2, UDI/DI 732094009057 8 73209400904034XFST-4, UDI/DI 732094009040 9 73209400903334XFST-6, UDI/DI 732094009033 10 73209400902634XFST-7, UDI/DI 732094009026 11 73209400885234XXST-2, UDI/DI 732094008852 12 73209400884534XXST-4, UDI/DI 732094008845 13 73209400883834XXST-6, UDI/DI 732094008838 14 73209400882134XXST-7, UDI/DI 732094008821 15 732094072402PWCD-5WT-2, UDI/DI 732094072402 16 732094155808PWCD-5WT-4, UDI/DI 732094155808 17 732094072389PWCD-5WT-6, UDI/DI 732094072389 18 732094072365PWCD-5WT-7, UDI/DI 732094072365 19 732094347494PWCD-6WT-2, UDI/DI 732094347494 20 732094347470PWCD-6WT-6, UDI/DI 732094347470 - Amount recalled
- 11154 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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