FDA Device recall Z-2246-2016
DeVilbiss Model 7305P-D Powered Suction Unit
- FDA Device
- Class II
- terminated
- Published 2016-07-27
On 2016-07-27 the FDA classified a Class II recall of DeVilbiss Model 7305P-D Powered Suction Unit by Devilbiss Healthcare, citing A small percentage of units of 7305 Series Vacu-Aide Suction Units are experiencing premature failure during operation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2246-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-05-23 |
| Published | 2016-07-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Devilbiss Healthcare |
| Distribution | FL, IN, KY, LA, MN, MO, NC, OH, SC, TN, TX, WI |
Product
DeVilbiss Model 7305P-D Powered Suction Unit
Reason
A small percentage of units of 7305 Series Vacu-Aide Suction Units are experiencing premature failure during operation.
Identifiers
| code_info | Serial numbers: PD465146 - PD465193 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2246-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.