DeVilbiss Vacu-Aide QSU Suction Unit — Class II medical device recall Z-2319-2013
Terminated recall by DeVilbiss Healthcare LLC, reported 2013-10-09. End users of the DeVilbiss Disposable Suction Container/Filter had exposed the bacterial filter cartridge to f
| Recall number | Z-2319-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DeVilbiss Healthcare LLC, Somerset, PA, United States |
| Recall initiated | 2013-03-07 |
| Classified | 2013-09-30 |
| Reported by FDA | 2013-10-09 |
| Terminated | 2014-11-06 |
| Countries outside the US | CA, MX |
| Quantity | 112,849 |
| Reason classes | microbial contamination |
| Model numbers | 7305D-632, 7305D-633, 7305D-633-25, 7305D-634 |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2319-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.