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

Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Single Spike, Ref ASC1200, packaged 1/box, 12 boxes/case, single use, RX, Sterile. — recall Z-2486-2018

U.S. FDA — Device Enforcement · United States · 2018-06-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2486-2018
Date of alert
2018-06-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardinal Health 200, LLC
Product category
device
Product type
Devices
Reported risk: The suction valve may not close properly which could cause continuous suction.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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.