Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd. Due to Spacelabs has received reports of the Arkon Anesthesia...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Del Mar Reynolds Medical, Ltd. directly.
Affected Products
Arkon Anesthesia Delivery System, Model 99999. Product Usage: Continuous Ventilator The Arkon Anesthesia Delivery System is designed to provide emergency oxygen, vaporized agent delivery and manual ventilation in the event of a power failure scenario. Clinicians are able to use Emergency O2 and manually ventilate the patient, providing gas and agent. However, the anesthesiologist will not have access to mechanical ventilation or ventilator monitoring.
Quantity: 325 devices sold to 35 US consignees and 76 devices sold to 14 international consignees
Why Was This Recalled?
Spacelabs has received reports of the Arkon Anesthesia Delivery System, Model 99999, shutting down without warning. The power supply has failed in a way that does not trigger the normal on battery alarms.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Del Mar Reynolds Medical, Ltd.
Del Mar Reynolds Medical, Ltd. has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report