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

Recall Z-1158-2023 — Cardinal Health Presource Packs IV START TRAY I-Intended for IV access device CATALOG #: 01-5799A

U.S. FDA — Device Enforcement · United States · 2022-11-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1158-2023
Date of alert
2022-11-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardinal Health 200, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
50195594381965
Reported risk: Presource Kits contains the ICU MicroClave Clear Connector due to a manufacturing defect there is a gap between the connectors top and bottom housings which may lead to fluid leaks and loss of fluid path integrity
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.