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

Recall Z-0186-2024 — Alaris PCA Module 8120

U.S. FDA — Device Enforcement · United States · 2023-09-15 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0186-2024
Date of alert
2023-09-15
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
CareFusion 303, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10885403516023
Reported risk: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.