Class II — Zeiss, Carl Inc
| Recalling firm | Carl Zeiss Inc. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Under certain circumstances, the firmware makes it possible for the Disinfection unit UV (432332-9020-000) to activate outside of the Celldiscoverer 7 housing. This may result in exposure of the users to harmful UV radiation. |
| Product | Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope |
| Quantity | 8 |
| Distribution | US Nationwide Distribution |
| Initiated | 2018-05-29 |
| Classified | 2018-07-19 |
| Terminated | 2024-07-26 |
| Recall number | Z-2441-2018 |
| Initiation | FDA Mandated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Zeiss, Carl Inc (Z-2441-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80418/
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