Medical device recalls Moderate risk

Advanced Sterilization Products recalls CIDEX Activated Dialdehyde Solution, 4 bottles/case, P/N: 2266

Recall date
July 27, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2459-2015
FDA classification
Class II
Brand / firm
Advanced Sterilization Products
Sold / distributed
US (nationwide) Distribution

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

CIDEX Activated Dialdehyde Solution, 4 bottles/case, P/N: 2266

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