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

Recall Z-2180-2025 — BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 SmartSite Y-sites LVP 60D DEHP FREE 3SS CV; REF: 2452-0007, BD Alaris Pump Infusion Set, 2 Back Check Valves, 3 SmartSite Y-sitesAS LVP 10D 3SS 2CV; REF: 2204-0007, BD Alaris Pump Infusion SetAS LVP

U.S. FDA — Device Enforcement · United States · 2025-07-08 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2180-2025
Date of alert: 2025-07-08
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: CareFusion 303, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10013186

Reported risk: Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.

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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