RegWardenFDA facility compliance records
Recall

Class II — DeVilbiss Healthcare LLC

Recalling firmDrive DeVilbiss Healthcare
Registered facilityDeVilbiss Healthcare LLC. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonA small percentage of units of 7305 Series Vacu-Aide Suction Units are experiencing premature failure during operation.
ProductDeVilbiss Model 7305P-D Powered Suction Unit
Quantity48 units
DistributionUS Distribution to the states of : NC, OH, TX, MO, TN, WI, KY, FL, LA, MN, IN, and SC
Initiated2016-05-23
Classified2016-07-20
Terminated2017-05-30
Recall numberZ-2246-2016
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — DeVilbiss Healthcare LLC (Z-2246-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/74308/

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