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

Recall Z-1236-2023 — CD5 Series of Genesis Reusable Rigid Sterilization Container Systems catalog number and product name: 1. CD5-3B, CONTAINER SHALLOW LG ENDO 3IN PERF; 2. CD5-3C, CONTAINER SHALLOW LG ENDO 3IN SOLID; 3. CD5-61B, GENESIS CONT LARGE ENDO PERF 28X11X6IN; 4. CD5-61C, GENESIS CONT LARGE ENDO SOLID

U.S. FDA — Device Enforcement · United States · 2023-01-30 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1236-2023
Date of alert: 2023-01-30
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Carefusion 2200 Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10885403019548

Reported risk: Product did not meet shelf-life testing requirements resulting in a breach of the sterility of the Genesis container holding surgical equipment.

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.

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