Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 145–156 of 2,088 recalls
Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
Device will intermittently provide inaccurate data related to native heart rate.
Device will intermittently provide inaccurate data related to native heart rate.
Potential for electrical discharge from unit when unplugged.
Devices could potentially be occluded or partially occluded.
Devices could potentially be occluded or partially occluded.
Software issue that can cause an increase in spontaneous software closures.
The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove o…
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.