CENTURION Vision System — Class II medical device recall Z-2081-2016
Terminated recall by Alcon Research, Ltd., reported 2016-07-06, distributed in IL. The grounding pin within the Power Entry Switch on certain systems was susceptible to detachment when the AC p
| Recall number | Z-2081-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Alcon Research, Ltd., Fort Worth, TX, United States |
| Recall initiated | 2016-05-24 |
| Classified | 2016-06-28 |
| Reported by FDA | 2016-07-06 |
| Terminated | 2017-04-13 |
| Distributed | IL |
| Quantity | 1 units |
| Reason classes | device malfunction |
| Serial numbers | 1601444801X |
Product
CENTURION Vision System
Reason for recall
The grounding pin within the Power Entry Switch on certain systems was susceptible to detachment when the AC power cable is removed.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2081-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.