Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2276-2012 — CIDEX OPA, High Level Disinfectant Solution, Glutaraldehyde-free (0.55% ortho-phthaladehyde) solution. The CIDEX OPA solution is intended for automated and manual cleaning and disinfection.

U.S. FDA — Device Enforcement · United States · 2012-06-01 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2276-2012
Date of alert: 2012-06-01
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Advanced Sterilization Products
Product category: device
Product type: Devices

Reported risk: The recall was initiated because Advanced Sterilization Products has discovered instances of missing labels on bottles of CIDEX OPA Solution, Part # 20390 manufactured between May 2011 and April 2012.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-2276-2012 — CIDEX OPA, High Level Disinfectant Solution, Glutaraldehyde-free (0.55% ortho-phthaladehyde) solution. The CIDEX OPA solution is intended for automated and manual cleaning and disinfection.

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