CIDEX Activated Dialdehyde Solution — Class II medical device recall Z-2459-2015
Terminated recall by Advanced Sterilization Products, reported 2015-09-02, distributed nationwide. Advanced Sterilization Products (ASP) is recalling the CIDEX Activated Dialdehyde Solution because it may lack
| Recall number | Z-2459-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advanced Sterilization Products, Irvine, CA, United States |
| Recall initiated | 2015-07-27 |
| Classified | 2015-08-25 |
| Reported by FDA | 2015-09-02 |
| Terminated | 2016-07-06 |
| Distributed | Nationwide (US) |
| Quantity | 23,426 cases |
Product
CIDEX Activated Dialdehyde Solution, 4 bottles/case, P/N: 2266
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2459-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.