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

Recall Z-0095-2020 — CVC TRIPLE LUMEN SAFETY BUNDLE ECVC6070

U.S. FDA — Device Enforcement · United States · 2019-04-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0095-2020
Date of alert
2019-04-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Centurion Medical Products Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
2018081550
Reported risk: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
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.