[Recalled] STERRAD Cyclesure Biological Indicator (BI, Part No. 14324. Intended to be used as a standard method for frequent monitoring of the STERRAD Sterilization System cycles. — Advanced Sterilization Products (ASP) is recalling the
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | STERRAD Cyclesure Biological Indicator (BI, Part No. 14324. Intended to be used as a standard method for frequent monitoring of the STERRAD Sterilization System cycles. |
|---|---|
| Brand / manufacturer | Advanced Sterilization Products |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0604-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 26 November 2013 |
| EAN / barcode | 14913706 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Advanced Sterilization Products (ASP) is recalling the STERRAD Cyclesure Biological Indicator (BI) because ASP has identified a microscopic intermittent and low frequency flaw in the outer vial of the STERRAD Cyclesure 24 Biological Indicator.
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.