Drug recall
CIDEX Activated Dialdehyde Solution, 4 bottles/case, P/N: 2266
FDA recall event 71708 · Class II · Advanced Sterilization Products
Key facts
| Event ID | 71708 |
|---|---|
| Recall numbers | Z-2459-2015 |
| Recalling firm | Advanced Sterilization Products |
| Product type | Devices |
| Products | CIDEX Activated Dialdehyde Solution, 4 bottles/case, P/N: 2266 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Advanced Sterilization Products (ASP) is recalling the CIDEX Activated Dialdehyde Solution because it may lack the adequate data to support the entire 24-month shelf life. |
| Initiation date | Jul 27, 2015 |
| Report date | Sep 2, 2015 |
| Termination date | Jul 6, 2016 |
| City | Irvine |
| State | CA |
| Country | United States |
| FEI number | 3003662624 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: