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Baxter Healthcare Corporation: Hillrom Welch Allyn Connex ProBP 3400 Digital

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: 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.. Recalled by Baxter Healthcare Corporation. Distribution: Global, US: NY, IL. Classification (Class II — potential health risk). Affected lots/dates: a) 34BFST-2, UDI/DI 732094009385; b) 34BFST-4, UDI/DI 732094009378; c) 34BFST-6, UDI/DI 732094009361; d) 34BXST-2, UD. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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