Baxter Healthcare Corporation is recalling 16,039 units of various medical devices, including Hillrom Welch Allyn Connex ProBP 3400 Digital Blood Pressure Devices, Spot Vision Screeners, and individual power cords. The recall was initiated because the construction of the power cords does not meet required insulation ratings and international electrical safety standards. While the company has received reports of this issue, they are voluntarily recalling the affected equipment to prevent potential electrical hazards. Consumers and healthcare providers should check their equipment against the specific model and UDI/DI numbers provided.
The power cords do not meet the necessary electrical insulation standards, which could lead to an electrical failure or shock hazard during use. This pose a risk of injury to both healthcare professionals and patients if the insulation fails to protect against the high-voltage current.
Manufacturer correction or instruction
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
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Sources: FDA iRES · Raw API Response
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