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

Recall Z-1759-2022 — BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171

U.S. FDA — Device Enforcement · United States · 2022-08-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1759-2022
Date of alert
2022-08-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CAREFUSION
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10885403237669
Reported risk: Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.
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.