[Recalled] STERRAD NX Sterilization System, Product Code: 10033, 10033-002 — Advanced Sterilization Products (ASP) has identified that in a rare sequence of… | FDA 2017-01-09
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | STERRAD NX Sterilization System, Product Code: 10033, 10033-002 |
|---|---|
| Brand / manufacturer | Advanced Sterilization Products |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1197-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 09 January 2017 |
| EAN / barcode | 33100270 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Advanced Sterilization Products
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.