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

Recall Z-0212-2023 — CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD3-4ST

U.S. FDA — Device Enforcement · United States · 2022-09-26 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0212-2023
Date of alert
2022-09-26
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Carefusion 2200 Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10885403019319
Reported risk: Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
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.

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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.