FDA Device recall Z-2081-2016
CENTURION Vision System
- FDA Device
- Class II
- terminated
- Published 2016-07-06
On 2016-07-06 the FDA classified a Class II recall of CENTURION Vision System by Alcon Research, citing the grounding pin within the Power Entry Switch on certain systems was susceptible to detachment when the AC power cable is removed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2081-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-05-24 |
| Published | 2016-07-06 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Alcon Research |
| Distribution | IL |
Product
CENTURION Vision System
Reason
The grounding pin within the Power Entry Switch on certain systems was susceptible to detachment when the AC power cable is removed.
Identifiers
| code_info | Serial Number 1601444801X |
|---|
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-2081-2016%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.