FDA Device recall Z-0419-2016
Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column
- FDA Device
- Class II
- terminated
- Published 2015-12-23
On 2015-12-23 the FDA classified a Class II recall of Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column by Teleflex Medical, citing product is being recalled due to complaints that the inspiratory and expiratory tubes are transposed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0419-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-17 |
| Published | 2015-12-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex Medical |
| Distribution | AL, AZ, CA, GA, IL, KY, LA, MA, MI, MN, NC, NJ, NY, OH, OK, OR, PA, TN, TX, WA |
Product
Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column
Reason
Product is being recalled due to complaints that the inspiratory and expiratory tubes are transposed.
Identifiers
| code_info | Lot Numbers : 02K1300128 and 02L1302324 |
|---|
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-0419-2016%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.