GE HealthCare Recalls Certain Carestation Devices Over Ventilation Risk
The Carestation anesthesia systems are being recalled due to a risk of ineffective ventilation in volume control mode, which could lead to serious injury or death.
Read MoreJun 23, 2025 | Anesthesia | 0 |
The Carestation anesthesia systems are being recalled due to a risk of ineffective ventilation in volume control mode, which could lead to serious injury or death.
Read MoreCustomers are being asked to remove the affected devices from use and replace with an alternate means of ventilation.
Read MoreCertain Z-800 series infusion pumps may malfunction due to unverified software, prompting a Class I recall by the FDA.
Read MoreIssues may cause therapy delays, false alarms, or thermal damage, though no injuries reported to date.
Read MoreWhile total recalls and units affected declined in Q1 2025, the number of Class I events increased.
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