Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
STERRAD NX Sterilization System Recalled by Advanced Sterilization Products Due to Advanced Sterilization Products (ASP) has identified that in...
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 Advanced Sterilization Products directly.
Affected Products
STERRAD NX Sterilization System, Product Code: 10033, 10033-002
Quantity: 7,694 units total (5,935 units in US)
Why Was This Recalled?
Advanced Sterilization Products (ASP) has identified that in a rare sequence of events following an external power outage, the system door interlock can be become disengaged during system reboot for a 20-second duration.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Advanced Sterilization Products
Advanced Sterilization Products has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report