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

Recall Z-2319-2013 — DeVilbiss Vacu-Aide QSU Suction Unit (Disposable Suction Container/Filter), 800 ML DISP Container, Unassembled, 800 ML DISP Container w/6' patient tubing, and 800 ML DISP Container w/6' patient tubing, assembled. DeVilbiss Vacu-Aide QSU Suction Unit (Disposable Suction Container/Filter) is used t

U.S. FDA — Device Enforcement · United States · 2013-03-07 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2319-2013
Date of alert: 2013-03-07
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: DeVilbiss Healthcare LLC
Product category: device
Product type: Devices

Reported risk: End users of the DeVilbiss Disposable Suction Container/Filter had exposed the bacterial filter cartridge to fluid, thereby occluding the filter and rendering it unusable.

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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