RecallRadar

FDA Device 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'…

On 2013-10-09 the FDA classified a Class II recall of DeVilbiss Vacu-Aide QSU Suction Unit (Disposable Suction Container/Filter), 800 ML DISP Container, Unassembled, 800 ML DISP Container w/6'… by Devilbiss Healthcare, citing 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.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2319-2013
ClassificationClass II
Statusterminated
Initiated2013-03-07
Published2013-10-09
Last updated2026-09-13 11:53 UTC
CompanyDevilbiss Healthcare
Distributionn/a

Product

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 to remove fluids from the airway or respiratory support system and infectious materials from wounds. It is available for use by consumers by physician order.

Reason

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.

Identifiers

code_infoPart Number 7305D-634 with model numbers 7305D-632, 7305D-633, and 7305D-633-25

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2319-2013%22

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