FDA Device recall Z-0396-2022
VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX
- FDA Device
- Class II
- terminated
- Published 2021-12-29
On 2021-12-29 the FDA classified a Class II recall of VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX by Civco Medical Instruments, citing there is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0396-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-10-08 |
| Published | 2021-12-29 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Civco Medical Instruments |
| Distribution | US |
Product
VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX
Reason
There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
Identifiers
| code_info | Part Number 610-1153; UDI 00841436102285; Lot Numbers: A122182, A131167, A131689, A131691, A141823 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Other recalls by Civco Medical Instruments
- eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158
FDA Device · Class II · 2026-04-08 · Civco Medical Instruments - eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
FDA Device · Class II · 2026-04-08 · Civco Medical Instruments - eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157
FDA Device · Class II · 2026-04-08 · Civco Medical Instruments - eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150
FDA Device · Class II · 2026-04-08 · Civco Medical Instruments - eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151
FDA Device · Class II · 2026-04-08 · Civco Medical Instruments
All Civco Medical Instruments recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0396-2022%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.