Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Dr¿ger Perseus A500 Anesthesia Workstation Recalled by Draeger Medical, Inc. Due to Unexpected shutdown while operating on battery power.
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 Draeger Medical, Inc. directly.
Affected Products
Dr¿ger Perseus A500 Anesthesia Workstation
Quantity: 16,841 units
Why Was This Recalled?
Unexpected shutdown while operating on battery power.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Draeger Medical, Inc.
Draeger Medical, Inc. has 78 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report