Intersurgical Inc recalls One-Piece Guedel Airway
Devices could potentially be occluded or partially occluded.
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Showing 85–96 of 4,932 recalls
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.
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.