Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Spacelabs BleaseSirius Anesthesia Workstation Recalled by Del Mar Reynolds Medical, Ltd. Due to A defect in CAS I/II Absorbers in the...
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 BleaseSirius Anesthesia Workstation, BleaseFocus Anesthesia Workstation, and CAS I/II Absorber contained in Service Kits Part Number 12200902, 050-0659-00 and 050-0901-00 and any workstation installed with the CAS I/II Absorber. Anesthesia workstation for use in the hospital environment and locations not requiring portability.
Quantity: 108 total (17 units in the US and 91 units outside the US)
Why Was This Recalled?
A defect in CAS I/II Absorbers in the Spacelabs Anesthesia Workstations and Service Kits may cause a condition leading to an increase in the carbon dioxide concentration within the inspired gas being delivered to the patient.
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