Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Spacelabs Healthcare Arkon Anesthesia Delivery System is intended for use Recalled by Del Mar Reynolds Medical, Ltd. Due to Reports of the Canister Carrier breaking during absorbent...
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
Spacelabs Healthcare Arkon Anesthesia Delivery System is intended for use in the hospital environment and operating room. Absorber Adapter Assembly Service Kit, part number: 050-9045-00. Absorber Adapter Assembly, part number: 650-1648-01. Arkon Absorber Canister Carrier, part number: 380-0916-01.
Quantity: 62 total (US= 19 devices and 32 kits; International = 11 devices)
Why Was This Recalled?
Reports of the Canister Carrier breaking during absorbent exchange or during anesthesia machine transit, causing a leak in the breathing circuit, which could cause hypoventilation in the patient.
Where Was This Sold?
This product was distributed to 6 states: FL, LA, MS, NC, SC, WY
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