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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

37,779 Total Recalls

Exposure of the UroPass product to Ultraviolet ( UV ) Radiation can cause brittleness of the device dilator tip, which may lead to broken dilator tips in the package or in patients during surgical procedures.

Sep 11, 2024 Other Medical Devices Nationwide View Details →

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

Oct 7, 2024 Infusion Pumps Nationwide View Details →

There is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries

Oct 4, 2024 Surgical Instruments Nationwide View Details →